Identity
- Trade Name
- SCANLAN® Titanium Forceps FDA UDI
- Generic Name
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
- Device Name
- S LEG Mic fcp, RH, NS DG, 1.0 mm tap DeBakey tips, 10"/25 cm FDA UDI
- Model / Reference
- 3003-938 FDA UDI
- Description
- S LEG Mic fcp, RH, NS DG, 1.0 mm tap DeBakey tips, 10"/25 cm FDA UDI
Identifiers
- Catalog Number
- 3003-938 FDA UDI
- Primary DI / UDI-DI
- 00846159003963 FDA UDI
- FDA Product Code
- GZX FDA UDI
- GMDN Term
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.4525 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical soft-tissue manipulation forceps, tweezers-like, reusable
SCANLAN® Titanium Forceps by Scanlan International Inc — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Scanlan International Inc
Sources (1)
- FDA UDI 1a9a77ef-2b01-406f-916a-94d3db7ba12e 35 fields · synced Jun 8, 2026