Identity
- Trade Name
- Instrument Set FDA UDI
- Generic Name
- Hand-held surgical retractor, reusable FDA UDI
- Device Name
- Single Pronge Large Hohmann Retrac. (35mm) FDA UDI
- Model / Reference
- Single Pronge Large Hohmann Retractor FDA UDI
- Description
- Single Pronge Large Hohmann Retrac. (35mm) FDA UDI
Identifiers
- Catalog Number
- 9095.10.561 FDA UDI
- Primary DI / UDI-DI
- 08033390064941 FDA UDI
- FDA Product Code
- LPH FDA UDIMBL FDA UDI
- GMDN Term
- Hand-held surgical retractor, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.3358 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
No
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
Instrument Set by Limacorporate — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Limacorporate
Sources (1)
- FDA UDI 6c2947b4-79a6-4dcb-8de5-be284d60426d 35 fields · synced Jun 1, 2026