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Cdi Medico Interantional

FDA UDI

Class I (US FDA UDI)

by Medico International Inc

Identity

Trade Name
CDI MEDICO INTERANTIONAL FDA UDI
Generic Name
Pressure bandage, non-latex, reusable FDA UDI
Device Name
BEIGE FACE WRAP, LARGE FDA UDI
Model / Reference
T-800C-B-L / T-124-L FDA UDI
Description
BEIGE FACE WRAP, LARGE FDA UDI

Identifiers

Catalog Number
T-124-L FDA UDI
Primary DI / UDI-DI
00850054025135 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

Cdi Medico Interantional 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 e11158fa-bd1c-4747-a134-8ec99c4da5c7 34 fields · synced Jun 8, 2026