Identity
- Trade Name
- Diamatrix FDA UDI
- Generic Name
- Eyelid speculum, reusable FDA UDI
- Device Name
- Lieberman Child lid speculum, Screw style adjustment for solid precise placement, This design is intended to lay over the temporal, Unique triple post speculum, 13mm small blades, Stainless Steel FDA UDI
- Model / Reference
- W20-13 FDA UDI
- Description
- Lieberman Child lid speculum, Screw style adjustment for solid precise placement, This design is intended to lay over the temporal, Unique triple post speculum, 13mm small blades, Stainless Steel FDA UDI
Identifiers
- Catalog Number
- W20-13 FDA UDI
- Primary DI / UDI-DI
- 00813059017215 FDA UDI
- FDA Product Code
- HNC FDA UDI
- GMDN Term
- Eyelid speculum, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 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
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Eyelid speculum, reusable
Diamatrix by Diamatrix — 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
- Diamatrix
Sources (1)
- FDA UDI d5282c55-3c2d-4eed-bd04-80d18b48113d 35 fields · synced May 30, 2026