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Medi

FDA UDI

Class I (US FDA UDI)

by Medi Manufacturing, Inc.

Identity

Trade Name
MEDI FDA UDI
Generic Name
Intestinal stoma shield/support belt, single-use FDA UDI
Device Name
!DO HERNIA SUPPORT BELT WHITE SIZE LG FDA UDI
Model / Reference
DP1AU73 FDA UDI
Description
!DO HERNIA SUPPORT BELT WHITE SIZE LG FDA UDI

Identifiers

Primary DI / UDI-DI
00636257204825 FDA UDI
FDA Product Code
IQE FDA UDI
GMDN Term
Intestinal stoma shield/support belt, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3490 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: Intestinal stoma shield/support belt, single-use

Medi by Medi Manufacturing, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intestinal stoma shield/support belt, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medi Manufacturing, Inc.

Sources (1)

  • FDA UDI 281e7b71-fe0a-457c-88a1-a4410e9bf253 34 fields · synced Jun 1, 2026