Identity
- Trade Name
- Diamatrix Ltd. FDA UDI
- Generic Name
- Eyelid speculum, reusable FDA UDI
- Device Name
- Barraquer lid speculum, .035" Stainless wire, This design is intended to lay over the bridge of the nose, 14mm Closed round blades, 18mm Blade spread, 39mm total length, Stainless FDA UDI
- Model / Reference
- W63 FDA UDI
- Description
- Barraquer lid speculum, .035" Stainless wire, This design is intended to lay over the bridge of the nose, 14mm Closed round blades, 18mm Blade spread, 39mm total length, Stainless FDA UDI
Identifiers
- Catalog Number
- W63 FDA UDI
- Primary DI / UDI-DI
- 00813059018892 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 Ltd. 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 c12f040d-975b-4ec4-920d-04e8f7080b0f 34 fields · synced Jun 6, 2026