Identity
- Trade Name
- Ahmed Tube Inserter FDA UDI
- Generic Name
- Ophthalmic implant handling forceps, reusable FDA UDI
- Device Name
- Tube Inserter FDA UDI
- Model / Reference
- TI FDA UDI
- Description
- Tube Inserter FDA UDI
Identifiers
- Catalog Number
- TI FDA UDI
- Primary DI / UDI-DI
- 00892064002331 FDA UDI
- FDA Product Code
- HNR FDA UDI
- GMDN Term
- Ophthalmic implant handling forceps, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 886.4350 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
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
MR Unsafe FDA UDI
Ahmed Tube Inserter by New World Medical, Incorporated — 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
- New World Medical, Incorporated
Sources (1)
- FDA UDI e17835d8-ed05-4ba2-afb3-cbf42e84cd82 36 fields · synced May 30, 2026