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DynaSafety Compress Gauze Roll Bandage, Sterile, 4" x 6yd

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
DynaSafety Compress Gauze Roll Bandage, Sterile, 4" x 6yd FDA UDI
Generic Name
Absorbent wound compression pad FDA UDI
Model / Reference
3197UB-1 FDA UDI

Identifiers

Primary DI / UDI-DI
00840117332690 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Absorbent wound compression pad FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 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

Yes

FDA UDI

Category: Absorbent wound compression pad

DynaSafety Compress Gauze Roll Bandage, Sterile, 4" x 6yd by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Absorbent wound compression pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 8202f42e-106d-4c25-aeb0-44f87d25d01b 32 fields · synced May 31, 2026