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DynaSafety Compress Bandages, 3", Offset, Sterile

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
DynaSafety Compress Bandages,3", Offset, Sterile FDA UDI
Generic Name
Absorbent wound compression pad FDA UDI
Device Name
Compress Bandages, Offset, Sterile, 3" FDA UDI
Model / Reference
3193 FDA UDI
Description
Compress Bandages, Offset, Sterile, 3" FDA UDI

Identifiers

Primary DI / UDI-DI
00616784319339 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

No

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 Bandages, 3", Offset, Sterile 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 91fcfe34-4c36-45b2-a61a-c48027357202 33 fields · synced May 30, 2026