Krinkle Gauze Roll, Non-Sterile

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name: Krinkle Gauze Roll, Non-Sterile FDA UDI
Generic Name: Woven gauze roll, non-sterile FDA UDI
Device Name: Krinkle Gauze Roll, Non-Sterile 4.5"x4.1yd, 6-ply FDA UDI
Model / Reference: 3162 FDA UDI
Description: Krinkle Gauze Roll, Non-Sterile 4.5"x4.1yd, 6-ply FDA UDI

Identifiers

Primary DI / UDI-DI: 00616784316239 FDA UDI
FDA Product Code: NAB FDA UDI
GMDN Term: Woven gauze roll, non-sterile 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Woven gauze roll, non-sterile

Krinkle Gauze Roll, Non-Sterile by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Dynarex Corp.

Sources (1)

FDA UDI 29d49477-3ff2-43bd-897a-c7b4df5c6062 33 fields · synced May 29, 2026