Identity
- Trade Name
- Ultracell FDA UDI
- Generic Name
- Ophthalmic sponge FDA UDI
- Device Name
- Cellulose Eye Spears FDA UDI
- Model / Reference
- NS40410Z FDA UDI
- Description
- Cellulose Eye Spears FDA UDI
Identifiers
- Primary DI / UDI-DI
- 30886158012673 FDA UDI
- FDA Product Code
- HOZ FDA UDI
- GMDN Term
- Ophthalmic sponge FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.4790 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Category: Ophthalmic sponge
Ultracell by Beaver-Visitec International, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic sponge.
- NETCELL — Network Medical Products, Ltd. · Class II
- NETCELL — Network Medical Products, Ltd. · Class II
- Eyetec — Network Medical Products, Ltd. · Class II
- Coronet — Network Medical Products, Ltd. · Class II
- Kitpack — Network Medical Products, Ltd. · Class II
- Sugi — QuestAlpha GmbH & Co. KG · Class II
- Coronet — Network Medical Products, Ltd. · Class II
- LASIK Drain — Hurricane Medical · Class II
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Beaver-Visitec International, Inc.
Sources (1)
- FDA UDI cfa33057-e908-476a-8cc8-b199bbf5c753 35 fields · synced May 30, 2026