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Mck

FDA UDI

Class I (US FDA UDI)

by GRI Medical & Electronic Technology Co., Ltd.

Identity

Trade Name
MCK FDA UDI
Generic Name
Surgical towel FDA UDI
Device Name
Towel_Cotton_Blue_27inx17in(69cmx43cm)_Sterile_1ea/bag_80bag/cs FDA UDI
Model / Reference
16-6001-B FDA UDI
Description
Towel_Cotton_Blue_27inx17in(69cmx43cm)_Sterile_1ea/bag_80bag/cs FDA UDI

Identifiers

Primary DI / UDI-DI
16931918175294 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Surgical towel FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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: Surgical towel

Mck by GRI Medical & Electronic Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical towel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bef58ebb-29f1-4094-ba19-6568e027d2b8 34 fields · synced Sep 18, 2026