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Eyetec

FDA UDI

Class I (US FDA UDI)

by Network Medical Products, Ltd.

Identity

Trade Name
Eyetec FDA UDI
Generic Name
Ophthalmic sponge FDA UDI
Device Name
1-470 Wipe and Wick Bulk Packed 1 per Unit Non-sterile FDA UDI
Model / Reference
1-470 FDA UDI
Description
1-470 Wipe and Wick Bulk Packed 1 per Unit Non-sterile FDA UDI

Identifiers

Primary DI / UDI-DI
05056100707290 FDA UDI
FDA Product Code
KCN FDA UDI
GMDN Term
Ophthalmic sponge FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.5220 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

Yes

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

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

Similar devices

Also classified as Ophthalmic sponge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Network Medical Products, Ltd.

Sources (1)

  • FDA UDI 4ab5af3c-b615-45d0-a59d-c5e62d540f78 33 fields · synced Jun 8, 2026