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Medical Workshop

FDA UDI

Class I (US FDA UDI)

by Network Medical Products, Ltd.

Identity

Trade Name
Medical Workshop FDA UDI
Generic Name
Corneal punch set FDA UDI
Device Name
MW-4875 Corneal Trephine 8.75mm Pack of 1. Sterile Single Use FDA UDI
Model / Reference
MW-4875 FDA UDI
Description
MW-4875 Corneal Trephine 8.75mm Pack of 1. Sterile Single Use FDA UDI

Identifiers

Primary DI / UDI-DI
05056100706248 FDA UDI
FDA Product Code
HRH FDA UDI
GMDN Term
Corneal punch set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4350 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: Corneal punch set

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

Similar devices

Also classified as Corneal punch set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 07efbe36-7254-4b7d-9ec4-3d6db6652cf2 33 fields · synced May 30, 2026