Identity
- Trade Name
- Baleen FDA UDI
- Generic Name
- Surgical suction system collection container, single-use FDA UDI
- Device Name
- The Baleen polyp trap is a single use device used in the suction retrieval of endoscopically removed polyps. FDA UDI
- Model / Reference
- NBPT520 FDA UDI
- Description
- The Baleen polyp trap is a single use device used in the suction retrieval of endoscopically removed polyps. FDA UDI
Identifiers
- Catalog Number
- NBPT520 FDA UDI
- Primary DI / UDI-DI
- 10724995184527 FDA UDI
- FDA Product Code
- KDQ FDA UDI
- GMDN Term
- Surgical suction system collection container, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Surgical suction system collection container, single-use
Baleen by US Endoscopy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Surgical suction system collection container, single-use.
- BEMIS — BEMIS MANUFACTURING CO. · Class II
- Bemis — BEMIS MANUFACTURING CO. · Class II
- Berkeley Vacurette — Gyrus Acmi, Inc. · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class II
- Oxygen Tubing Y-Connector — SUNSET HEALTHCARE SOLUTIONS, Inc. · Class II
- SOMAVAC Waste Collection Unit — SOMAVAC MEDICAL SOLUTIONS, INC. · Class I
- Bemis — BEMIS MANUFACTURING CO. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- US Endoscopy
Sources (1)
- FDA UDI 95b38a3b-4a9d-4f6f-8902-8a3b83675764 36 fields · synced Jun 8, 2026