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Medico International

FDA UDI

Class I (US FDA UDI)

by Medico International Inc

Identity

Trade Name
MEDICO INTERNATIONAL FDA UDI
Generic Name
Pressure bandage, non-latex, reusable FDA UDI
Device Name
LATEX-FREE GEL PACK SLEEVE, WHITE FDA UDI
Model / Reference
T-470 FDA UDI
Description
LATEX-FREE GEL PACK SLEEVE, WHITE FDA UDI

Identifiers

Catalog Number
T-470 FDA UDI
Primary DI / UDI-DI
00850054025005 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

Medico International 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 9751b78b-3b75-4ecf-ad9e-704e98d7df3d 35 fields · synced Jun 8, 2026