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ContourMD

FDA UDI

Class I (US FDA UDI)

by ContourMD Marketing Group, LLC

Identity

Trade Name
ContourMD FDA UDI
Generic Name
Perineal/coccygeal cushion FDA UDI
Device Name
BBL Pillow Post Surgery Lipo Foam 3 Sheet, BBL Brazilian Butt Lift Pillow ? Booty Pillow After Surgery with 3 Pack LipoFoam FDA UDI
Model / Reference
LIP-03-BBL FDA UDI
Description
BBL Pillow Post Surgery Lipo Foam 3 Sheet, BBL Brazilian Butt Lift Pillow ? Booty Pillow After Surgery with 3 Pack LipoFoam FDA UDI

Identifiers

Catalog Number
LIP-03-BBL FDA UDI
Primary DI / UDI-DI
00840425320723 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Perineal/coccygeal cushion FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Exudate-absorbent dressing, non-gel, non-antimicrobialPerineal/coccygeal cushion

ContourMD by ContourMD Marketing Group, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Perineal/coccygeal cushion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 75f0cfa2-92b8-4281-8517-48e5ffd76ef0 35 fields · synced Jun 1, 2026