Identity
- Trade Name
- Diamatrix FDA UDI
- Generic Name
- Ocular hook/spatula/manipulator, reusable FDA UDI
- Device Name
- Diamatrix Nucleus Chopper, Angled, Curved interior cutting edge with .5mm olive shaped tip, Intended to be used in the right hand, Slightly Angled 15mm from bend to tip, Round knurled Handle, 117mm total length, Stainless Steel FDA UDI
- Model / Reference
- H439-AR-S FDA UDI
- Description
- Diamatrix Nucleus Chopper, Angled, Curved interior cutting edge with .5mm olive shaped tip, Intended to be used in the right hand, Slightly Angled 15mm from bend to tip, Round knurled Handle, 117mm total length, Stainless Steel FDA UDI
Identifiers
- Catalog Number
- H439-AR-S FDA UDI
- Primary DI / UDI-DI
- 00813059014634 FDA UDI
- FDA Product Code
- HNQ FDA UDI
- GMDN Term
- Ocular hook/spatula/manipulator, 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: Ocular hook/spatula/manipulator, 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 7e200b8c-278d-4381-8f7b-0753f2a62b64 34 fields · synced May 30, 2026