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Catalyst Non-Expandable Bed

FDA UDI

Class II (US FDA UDI)

by Kreg Medical, Inc.

Identity

Trade Name
CATALYST NON-EXPANDABLE BED FDA UDI
Generic Name
Bariatric bed FDA UDI
Device Name
Hospital Bed with Standing Frame FDA UDI
Model / Reference
ASM100113 FDA UDI
Description
Hospital Bed with Standing Frame FDA UDI

Identifiers

Primary DI / UDI-DI
00850520008143 FDA UDI
FDA Product Code
FNL FDA UDI
GMDN Term
Bariatric bed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5100 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

No

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

Yes

FDA UDI

Category: Basic electric hospital bedBariatric bedBed mattress support platform, electricStand-up bed

Catalyst Non-Expandable Bed by Kreg Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stand-up bed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kreg Medical, Inc.

Sources (1)

  • FDA UDI e8b876e6-46fa-4318-8881-1cf1c1f5231c 34 fields · synced May 29, 2026