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Desmarres (12 mm) Stainless Steel Retractor for Laser (non glare)
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Desmarres (12 mm) Stainless Steel Retractor for Laser (non glare) FDA UDI
- Generic Name
- Hand-held surgical retractor, reusable FDA UDI
- Device Name
- The Desmarres is a retractor intended to retract tissue around the inferior eyelid's incision. The Desmarres has a shaft and its edge is a curved strip. The Desmarres can be used as a backstop to lay down tissue to excise with the laser. It is a smooth instrument that touches the patient's tissue, the shield or the eyelids. FDA UDI
- Model / Reference
- 21-312 FDA UDI
- Description
- The Desmarres is a retractor intended to retract tissue around the inferior eyelid's incision. The Desmarres has a shaft and its edge is a curved strip. The Desmarres can be used as a backstop to lay down tissue to excise with the laser. It is a smooth instrument that touches the patient's tissue, the shield or the eyelids. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10697660002092 FDA UDI
- FDA Product Code
- GAD FDA UDI
- GMDN Term
- Hand-held surgical retractor, reusable 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
Dimensions & Sizes
- Size
- Width — 12 Millimeter FDA UDI
Desmarres (12 mm) Stainless Steel Retractor for Laser (non glare) 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 35121903-5911-4e35-b9bf-4d0c7bdb9e7e 36 fields · synced May 30, 2026