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Medi-Band

FDA UDI

Class I (US FDA UDI)

by Medi-Tech International Corporation

Identity

Trade Name
Medi-Band FDA UDI
Generic Name
Abdominal binder, single-use FDA UDI
Device Name
Medi-Band Seamless Tubular Band Precut - Size 12 IN x 16 IN FDA UDI
Model / Reference
MBF261216 FDA UDI
Description
Medi-Band Seamless Tubular Band Precut - Size 12 IN x 16 IN FDA UDI

Identifiers

Catalog Number
MBF261216 FDA UDI
Primary DI / UDI-DI
00027479270062 FDA UDI
FDA Product Code
ISR FDA UDI
GMDN Term
Abdominal binder, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3025 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

No

FDA UDI

Combination Product

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Abdominal binder, single-use

Medi-Band by Medi-Tech International Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal binder, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 32c928ef-f1eb-46c9-a46a-246a479fddaf 35 fields · synced Jun 8, 2026