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Kolbs

FDA UDI

Class I (US FDA UDI)

by K2 Health Products

Identity

Trade Name
Kolbs FDA UDI
Generic Name
Gel-filled bed mattress overlay FDA UDI
Device Name
Kolbs Gel Overlay FDA UDI
Model / Reference
KGELO FDA UDI
Description
Kolbs Gel Overlay FDA UDI

Identifiers

Primary DI / UDI-DI
00816554010378 FDA UDI
FDA Product Code
IKY FDA UDI
GMDN Term
Gel-filled bed mattress overlay FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5150 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Gel-filled bed mattress overlay

Kolbs by K2 Health Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gel-filled bed mattress overlay.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
K2 Health Products

Sources (1)

  • FDA UDI 5e003543-b3d6-4941-958c-49f14e46b640 34 fields · synced May 30, 2026