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Belly Bandit

FDA UDI

Class I (US FDA UDI)

by The Ergo Baby Carrier, Inc.

Identity

Trade Name
Belly Bandit FDA UDI
Generic Name
Pressure bandage, non-latex, single-use FDA UDI
Device Name
C-Section Recovery Undies - Almond - XL FDA UDI
Model / Reference
90026 FDA UDI
Description
C-Section Recovery Undies - Almond - XL FDA UDI

Identifiers

Catalog Number
CSECUNNUDE:XL FDA UDI
Primary DI / UDI-DI
00191653900264 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Pressure bandage, non-latex, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 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

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: Pressure bandage, non-latex, single-use

Belly Bandit by The Ergo Baby Carrier, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure bandage, non-latex, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 66028365-911a-43e2-8599-dfee38a21c1e 34 fields · synced Jun 8, 2026