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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
Medical device cleaning sponge/set FDA UDI
Device Name
Carton Label - Diamond Knife Cleaning Block FDA UDI
Model / Reference
40-462-USA FDA UDI
Description
Carton Label - Diamond Knife Cleaning Block FDA UDI

Identifiers

Primary DI / UDI-DI
05060165016990 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Medical device cleaning sponge/set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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: Medical device cleaning sponge/set

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

Similar devices

Also classified as Medical device cleaning sponge/set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a2606444-450c-4a54-b5f8-685aade1520b 33 fields · synced Jun 8, 2026