Clinical Utilization Management Guidelines (CUMG) list for DME and other services
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This document lists the Clinical Utilization Management Guidelines (CUMG) adopted by Simply Healthcare Plans, indicating guideline identifiers and titles across DME and other specialties; it governs medical necessity review and prior authorization processes used by Simply for applicable services.
No material clinical or coverage changes in this revision.
Coverage Criteria Overview
The CUMG listing references the externally published MCG Care Guidelines as an accepted source for select utilization reviews. MCG is applied only for: inpatient medical and behavioral health medical necessity review; assessment of inpatient site-of-service appropriateness; inpatient rehabilitation and skilled nursing facility review; and outpatient services or procedures when no other Simply Medical Policy or Clinical UM guideline exists. Medicaid state contracts, regulatory guidance, CMS requirements, and Simply's Medical Policy/Clinical UM Guidelines supersede MCG where applicable.
This section functions as an index of adopted Clinical Utilization Management Guidelines (CUMG/CG items) and lists guideline identifiers and titles (some marked as New). The indexed content is not a stand-alone statement of coverage, explicit coverage criteria, or exclusion rules; each listed CUMG references a separate guideline document that contains the detailed clinical criteria and coverage determinations.
Billing Codes and Code Lists
Provider Actions & Prior Authorization
Pre-payment review uses the CUMG (CG-ADMIN-01 precedence)
Pre-payment review and medical necessity determinations are performed using Simply's Clinical Utilization Management Guidelines (CUMG). When no other clinical UM guideline exists, CG-ADMIN-01 (Clinical Utilization Management Guideline for Pre-Payment Review Medical Necessity Determinations) is used to guide pre-payment review.
- MCG Care Guidelines are used only where no other clinical UM guideline exists for certain inpatient and outpatient reviews and are superseded by Medicaid state contracts, regulatory guidance, CMS requirements, and Simply's Medical Policy/Clinical UM Guidelines.
- Requests that do not meet established criteria will be referred to a licensed physician reviewer for determination.
CUMG index only — no explicit PA criteria listed
This section is an index that enumerates CUMG identifiers and titles (several items are marked “New”) rather than listing specific prior authorization criteria.
- The listing presents CUMG number and title pairs (e.g., CG-ADMIN-01) and flags new items where applicable.
- Providers must refer to the individual CUMG document for any specific authorization requirements.
Provider note: index of guidelines — consult individual CUMG for requirements
Providers should note that this document is an index of adopted CUMG items and that specific clinical or authorization requirements are contained in each individual guideline; consult the referenced guideline for required actions when submitting requests.
- The index lists CUMG identifiers and titles (many across specialties) but does not itself define authorization criteria.
- When submitting requests, reference the applicable CG-DME guideline for equipment-specific requirements and documentation standards.
Follow each CG-DME guideline for actionable requirements
Supplementary provider-facing instructions: this listing does not replace the full CG-DME guideline documents; providers must follow the specific CG-DME guideline for clinical criteria, documentation, and any authorization or rental/purchase rules.
- The document enumerates many CG-DME guideline identifiers and titles; equipment-specific rules (rental vs purchase, replacement intervals) are defined within each CG-DME guideline.
- If no specific CG-DME exists for a requested service, CG-ADMIN-01 guides pre-payment review.
Document medical necessity per Medicaid/CMS/ADMIN.00004 and the specific CG-DME
Medical necessity determinations are made on a case-by-case basis according to the definition of medical necessity contained within the Medicaid state contract, regulatory guidance, CMS requirements, or Simply's Medical Necessity Criteria Policy ADMIN.00004; refer to each CG-DME for item-specific documentation requirements.
- The CUMG list points to separate guideline documents that detail documentation requirements per equipment type (e.g., CG-DME-03, CG-DME-15, CG-DME-31).
- Providers must supply the documentation specified in the applicable CG-DME when requesting authorization or coverage determinations.
Sign up for provider communications for timely updates
Providers and members are encouraged to sign up to receive email updates (including some communications sent in lieu of fax or mail) via the QR code or online form at https://bit.ly/signup-sml-fl to receive timely policy and guideline notices.
- Email is the quickest way to receive important information from Simply; sign-up is optional and not a billing or documentation requirement.
Denial risk if request does not meet guideline criteria
Requests that do not meet the established guideline criteria will be referred to a licensed physician reviewer with appropriate clinical expertise and may be denied if the medical necessity definition criteria are not met.
- Nonconforming requests may result in denial following physician review.
- Providers should ensure submissions conform to the applicable CUMG or, if none exists, to CG-ADMIN-01 to avoid referral and potential denial.
Index only — no explicit authorization/denial criteria in this listing
This document functions as an index of CUMG items and does not itself provide explicit authorization or denial criteria; providers must consult the referenced guideline for actionable authorization rules.
- The listing enumerates CUMG numbers and titles (some marked New) but contains no explicit coverage or denial logic.
- For authorization decisions, use the applicable CG-DME or CG-ADMIN-01 when no other guideline exists.
Background & Scope
This document catalogues the Clinical Utilization Management Guidelines (CUMGs) adopted by Simply to support utilization management decisions. The CUMG list is used to guide medical necessity and prior authorization reviews; determinations are made on a case-by-case basis in accordance with the definition of medical necessity contained in the applicable Medicaid state contract, regulatory guidance, CMS requirements, or Simply's Medical Necessity Criteria Policy (ADMIN.00004). When a request does not meet established guideline criteria, it will be referred to a licensed physician reviewer for final determination.
Definitions
Medical Necessity Approach for DME
DME medical necessity approach
Coverage and medical necessity determinations for DME referenced in this list are governed by the specific CG-DME guideline for each equipment type and by Medicaid/CMS requirements.
If a request does not meet established guideline criteria it will be referred to a licensed physician reviewer with appropriate clinical expertise; refer to the individual CG-DME guideline for item-specific clinical criteria and documentation requirements.
Rental, Purchase, and Equipment Rules
| Equipment / DME category | Referenced CG-DME guideline ID |
|---|---|
| Neuromuscular Stimulation devices | |
| CG-DME-03 | |
| Electrical Nerve Stimulation (TENS) devices | |
| CG-DME-04 | |
| Cervical Traction Devices for Home Use | |
| CG-DME-05 | |
| Compression Devices for Lymphedema | |
| CG-DME-06 | |
| Augmentative and Alternative Communication (AAC) devices with digitized or synthesized speech output | |
| CG-DME-07 | |
| Infant Home Apnea Monitors | |
| CG-DME-08 | |
| Elastomeric Infusion Pumps (continuous local delivery of analgesia post-op) | |
| CG-DME-09 | |
| Durable Medical Equipment (general) | |
| CG-DME-10 | |
| Lower Limb Prosthesis | |
| CG-DME-13 | |
| Noninvasive Electrical Bone Growth Stimulators | |
| CG-DME-40 | |
| Ultraviolet Light Therapy Devices for Home Use | |
| CG-DME-41 | |
| Continuous Glucose Monitoring Devices | |
| CG-DME-42 | |
| High Frequency Chest Wall Oscillation / Clearance devices | |
| CG-DME-43 | |
| Tumor Treating Field (TTF) devices | |
| CG-DME-44 | |
| Pneumatic Compression Devices for DVT prevention (home) | |
| CG-DME-46 | |
| Noninvasive Home Ventilator Therapy for Respiratory Failure | |
| CG-DME-47 | |
| Vacuum Assisted Wound Therapy (outpatient/home) | |
| CG-DME-48 | |
| Standing Frames | |
| CG-DME-49 | |
| Automated Insulin Delivery Systems / External Insulin Pumps | |
| CG-DME-50 / CG-DME-51 |
Replacement & Repair
Documentation Requirements
Follow the CG‑DME guideline for equipment‑specific documentation
Refer to the specific CG‑DME guideline identified for the equipment being requested to determine the exact documentation required (e.g., CG‑DME‑03, CG‑DME‑15, CG‑DME‑31).
- Each CG‑DME guideline contains the equipment‑specific clinical criteria and documentation checklist providers must supply for authorization.
- Rental vs. purchase rules and replacement intervals are defined within the applicable CG‑DME guideline.
Communications sign‑up is optional (not a billing requirement)
Signing up for email communications is optional and intended for timely updates; it is not a billing or documentation requirement for claims or authorizations.
- Use the QR code or https://bit.ly/signup-sml-fl to enroll; enrollment does not change documentation or billing obligations.
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