Identity
- Trade Name
- NETWORK FDA UDI
- Generic Name
- Ophthalmic sponge FDA UDI
- Device Name
- NS40300 PVA Spears Non-sterile 5 Piece FDA UDI
- Model / Reference
- NS40300 FDA UDI
- Description
- NS40300 PVA Spears Non-sterile 5 Piece FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05056100706996 FDA UDI
- 510(k) Number
- K130117 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
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Ophthalmic sponge
Network by Network Medical Products, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Ophthalmic sponge.
- Ultracell — Beaver-Visitec International, Inc. · Class II
- Visitec® — Beaver-Visitec International, Inc. · Class II
- Ultracell — Beaver-Visitec International, Inc. · Class II
- Sugi — QuestAlpha GmbH & Co. KG · Class II
- Ultracell — Beaver-Visitec International, Inc. · Class II
- LASIK Drain — Hurricane Medical · Class II
- PRO-PAKS®️ — MICROSPECIALITIES, INC. · Class II
- Merocel — Beaver-Visitec International, Inc. · Class II
Cleared under the same submission
K130117 also covers:
- Coronet — Network Medical Products, Ltd.
- Coronet — Network Medical Products, Ltd.
- Coronet — Network Medical Products, Ltd.
- Coronet — Network Medical Products, Ltd.
- Coronet — Network Medical Products, Ltd.
- Coronet — Network Medical Products, Ltd.
- Eyetec — Network Medical Products, Ltd.
- Eyetec — Network Medical Products, Ltd.
- Eyetec — Network Medical Products, Ltd.
- Eyetec — Network Medical Products, Ltd.
- Eyetec — Network Medical Products, Ltd.
- Eyetec — Network Medical Products, Ltd.
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
- Network Medical Products, Ltd.
Sources (1)
- FDA UDI acc95c87-2349-4c03-87b9-506de3388036 34 fields · synced Jun 8, 2026