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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
Lumbar cushion FDA UDI
Device Name
Lipo Lumbar Molder Backboard Liposuction BBL Post Surgery FDA UDI
Model / Reference
Purchased:CMD-LUMBB-0S FDA UDI
Description
Lipo Lumbar Molder Backboard Liposuction BBL Post Surgery FDA UDI

Identifiers

Catalog Number
Purchased:CMD-LUMBB-0S FDA UDI
Primary DI / UDI-DI
00840425320792 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Lumbar 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lumbar cushion

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

Similar devices

Also classified as Lumbar cushion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d60efd05-bab9-41ff-b3e2-af33f0b984a9 35 fields · synced Jun 8, 2026