Identity
- Trade Name
- Surgical Direct FDA UDI
- Generic Name
- Flexible endoscopic biopsy forceps, reusable FDA UDI
- Device Name
- Long Ellipsoid Fen Cup 1.8mm x 35cm FDA UDI
- Model / Reference
- SD5514 FDA UDI
- Description
- Long Ellipsoid Fen Cup 1.8mm x 35cm FDA UDI
Identifiers
- Catalog Number
- SD5514 FDA UDI
- Primary DI / UDI-DI
- B382SD55140 FDA UDI
- FDA Product Code
- GCJ FDA UDI
- GMDN Term
- Flexible endoscopic biopsy forceps, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Flexible endoscopic biopsy forceps, reusable
Surgical Direct by Surgical Direct, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Surgical Direct, Inc.
Sources (1)
- FDA UDI 061b8c1b-35cd-4d52-a037-63fe9972e5d3 35 fields · synced May 31, 2026