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Dealmed

FDA UDI

Class I (US FDA UDI)

by Dealmed Medical Supplies Llc

Identity

Trade Name
Dealmed FDA UDI
Generic Name
Non-adhesive device retention bandage FDA UDI
Device Name
Conforming Stretch Bandage N/S LF Polyester 4" x 4.1 yds 12/Box FDA UDI
Model / Reference
817415020161 FDA UDI
Description
Conforming Stretch Bandage N/S LF Polyester 4" x 4.1 yds 12/Box FDA UDI

Identifiers

Catalog Number
783104 FDA UDI
Primary DI / UDI-DI
00817415020154 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Non-adhesive device retention bandage 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-adhesive device retention bandage

Dealmed by Dealmed Medical Supplies Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-adhesive device retention bandage.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c3c888d9-2f6a-4ed7-aecf-34f4df07fde0 35 fields · synced Jun 8, 2026