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Medi-First Basic Plastic Burn Kit

FDA UDI

Class N (US FDA UDI)

by Medique Products

Identity

Trade Name
Medi-First Basic Plastic Burn Kit FDA UDI
Generic Name
Burn kit, non-medicated FDA UDI
Device Name
1 -Antiseptic Wipes, 10ct 1 -1” x 3” Plastic Strips, 16ct 2 -4" x 4" Burn Dressings 2 -2" x 6" Burn Dressings 4 -Water Jel Burn Jel 3.5gm Pkts 2 -Vinyl Exam Gloves, Disp., Pair 2 -2” Stretch Roller Gauze 1 -1/2” x 5yds Adhesive Tape 1 -Scissors, 4.5” 1- Instruction Sheet FDA UDI
Model / Reference
89610 FDA UDI
Description
1 -Antiseptic Wipes, 10ct 1 -1” x 3” Plastic Strips, 16ct 2 -4" x 4" Burn Dressings 2 -2" x 6" Burn Dressings 4 -Water Jel Burn Jel 3.5gm Pkts 2 -Vinyl Exam Gloves, Disp., Pair 2 -2” Stretch Roller Gauze 1 -1/2” x 5yds Adhesive Tape 1 -Scissors, 4.5” 1- Instruction Sheet FDA UDI

Identifiers

Catalog Number
89610 FDA UDI
Primary DI / UDI-DI
00347682896102 FDA UDI
FDA Product Code
OJI FDA UDI
GMDN Term
Burn kit, non-medicated FDA UDI

Classification

Device Class
N 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

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

Yes

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: Burn kit, non-medicated

Medi-First Basic Plastic Burn Kit by Medique Products — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Burn kit, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medique Products

Sources (1)

  • FDA UDI bebaf9a5-51e0-40ba-a17a-e39bff7b3419 36 fields · synced May 30, 2026