Identity
- Trade Name
- Biopsy Forceps FDA UDI
- Generic Name
- Flexible endoscopic biopsy forceps, single-use FDA UDI
- Device Name
- Endoscopic Biopsy Forceps with Needle FDA UDI
- Model / Reference
- SU-211-622 FDA UDI
- Description
- Endoscopic Biopsy Forceps with Needle FDA UDI
Identifiers
- Catalog Number
- SU-211-622 FDA UDI
- Primary DI / UDI-DI
- 00816207020808 FDA UDI
- FDA Product Code
- FCL FDA UDI
- GMDN Term
- Flexible endoscopic biopsy forceps, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.1075 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 2.4 Millimeter FDA UDILength — 230 Centimeter FDA UDI
Biopsy Forceps by Endo-Therapeutics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 I | Pending data |
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Manufacturer
- Manufacturer
- Endo-Therapeutics, Inc.
Sources (1)
- FDA UDI ecd1075a-eb81-447b-82f7-feffc989c2ea 38 fields · synced Jun 1, 2026