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Caromed

FDA UDI

Class I (US FDA UDI)

by Medico International Inc

Identity

Trade Name
CAROMED FDA UDI
Generic Name
Pressure bandage, non-latex, reusable FDA UDI
Device Name
CAROMED FACE-LIFT BANDAGE, CHAMPAGNE, LARGE FDA UDI
Model / Reference
T-800C-26-M / 1-8026M FDA UDI
Description
CAROMED FACE-LIFT BANDAGE, CHAMPAGNE, LARGE FDA UDI

Identifiers

Catalog Number
1-8026M FDA UDI
Primary DI / UDI-DI
00850054025050 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Pressure bandage, non-latex, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Pressure bandage, non-latex, reusable

Caromed by Medico International Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure bandage, non-latex, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3eea38ee-7928-4a33-9e5a-1e5a2cc219ca 35 fields · synced May 29, 2026