Summary & Overview
HCPCS C1738: Powered Single-Use Endoscopic Ultrasound-Guided Biopsy Device
HCPCS Level II code C1738 identifies a powered, single-use endoscopic ultrasound-guided biopsy device used to obtain tissue samples during EUS procedures. As EUS-guided tissue acquisition grows in diagnostic importance for gastrointestinal, pancreatic and thoracic lesions, clear coding for disposable biopsy devices supports accurate supply reporting and claims processing nationwide. This code matters for hospitals, ambulatory surgery centers, and endoscopy suites that supply devices as part of procedural episodes and for payers establishing coverage and payment policies.
Key payers in scope include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare and Medicare. Readers will find a concise synthesis of what the code represents, the clinical and site-of-service context, and the payer landscape covered. The publication summarizes expected use cases, common billing modifiers (listed separately), and where to find related coding and policy references. It is intended to help revenue cycle, coding, and clinical teams understand the administrative classification of a powered, disposable EUS biopsy device, how it fits into procedural supply reporting, and what payers typically consider when processing claims. Data not available in the input is noted where applicable.
Billing Code Overview
HCPCS Level II code C1738 describes a powered, single-use (disposable) endoscopic ultrasound-guided biopsy device. This device is intended for use during endoscopic ultrasound (EUS) procedures to obtain tissue samples from lesions or masses visualized via endoscopic ultrasound imaging.
Service type: EUS-guided biopsy device supply and procedural accessory
Typical site of service: Hospital outpatient department, ambulatory surgery center, or endoscopy suite
Clinical & Coding Specifications
Clinical Context
A 62-year-old patient with a history of chronic smoking and recent unexplained weight loss presents with a 2.5 cm submucosal mass in the posterior mediastinum identified on chest CT. The thoracic surgeon and pulmonologist coordinate an endoscopic ultrasound-guided tissue sampling to obtain diagnostic material for histology and molecular studies. The patient is scheduled to undergo conscious sedation in an ambulatory endoscopy suite. The procedure uses a C1738 powered, single-use endoscopic ultrasound-guided biopsy device to obtain core and/or needle biopsy specimens from the mediastinal mass via an endoscopic ultrasound (EUS) approach.
During the encounter the clinical workflow includes pre-procedure consent and time-out, topical and/or monitored anesthesia care, endoscopic ultrasound imaging to localize the lesion, deployment of the disposable powered biopsy device to obtain targeted samples, on-site specimen handling (slide preparation, cell block, and preservation for molecular testing), hemostasis if needed, and post-procedure recovery with discharge instructions. The device is billed as C1738 when a powered, single-use EUS-guided biopsy device is used for tissue acquisition during the endoscopic procedure.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
22 |