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Kitpack

FDA UDI

Class II (US FDA UDI)

by Network Medical Products, Ltd.

Identity

Trade Name
Kitpack FDA UDI
Generic Name
Ophthalmic sponge FDA UDI
Device Name
Wick and Wipe3"x3"x1mm Sterile FDA UDI
Model / Reference
2-469 FDA UDI
Description
Wick and Wipe3"x3"x1mm Sterile FDA UDI

Identifiers

Primary DI / UDI-DI
05056100712614 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

Kitpack by Network Medical Products, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic sponge.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a27491ea-236a-4f37-a7c3-247fe20b0dec 34 fields · synced Jun 1, 2026