Identity
- Trade Name
- Snowden-Pencer FDA UDI
- Generic Name
- Hand-held surgical retractor, reusable FDA UDI
- Device Name
- Snowden-Pencer Plastics RETRACTOR CONVERSE, WITH FIBER-OPTICS 5CM (2") TAPERED BLADE FDA UDI
- Model / Reference
- 88-1026 FDA UDI
- Description
- Snowden-Pencer Plastics RETRACTOR CONVERSE, WITH FIBER-OPTICS 5CM (2") TAPERED BLADE FDA UDI
Identifiers
- Catalog Number
- 88-1026 FDA UDI
- Primary DI / UDI-DI
- 10885403151330 FDA UDI
- FDA Product Code
- FDG FDA UDI
- GMDN Term
- Hand-held surgical retractor, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.4530 FDA UDI
- Commercial Distribution
- Not 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
Snowden-Pencer by Carefusion 2200, 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
- Carefusion 2200, Inc.
Sources (1)
- FDA UDI 3be6c247-905b-4a43-9b3c-43dfb9da27fa 36 fields · synced Sep 18, 2026