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Desmarres, Autoclavable plastic retractors t-yellow
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Desmarres, Autoclavable plastic retractors t-yellow FDA UDI
- Generic Name
- Hand-held surgical retractor, single-use FDA UDI
- Device Name
- Desmarres, Autoclavable plastic retractors transparent-yellow (2 models, 4 different ends) FDA UDI
- Model / Reference
- 23-310Y FDA UDI
- Description
- Desmarres, Autoclavable plastic retractors transparent-yellow (2 models, 4 different ends) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20697660003324 FDA UDI
- FDA Product Code
- GAD FDA UDI
- GMDN Term
- Hand-held surgical retractor, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
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
Desmarres, Autoclavable plastic retractors t-yellow by Oculo-Plastik 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
- Oculo-Plastik Inc
Sources (1)
- FDA UDI 9aaa8ccb-fc17-4f09-90fb-dacee00c3e45 35 fields · synced Jun 8, 2026