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Single Arm Trapeze Assembly

FDA UDI

Class I (US FDA UDI)

by Kreg Medical, Inc.

Identity

Trade Name
SINGLE ARM TRAPEZE ASSEMBLY FDA UDI
Generic Name
Bed traction frame FDA UDI
Device Name
Single Arm Trapeze FDA UDI
Model / Reference
ASM100105 FDA UDI
Description
Single Arm Trapeze FDA UDI

Identifiers

Primary DI / UDI-DI
00850520008006 FDA UDI
FDA Product Code
ILZ FDA UDI
GMDN Term
Bed traction frame FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5925 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: Bed traction frameTrapeze bar exerciser

Single Arm Trapeze Assembly by Kreg Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Trapeze bar exerciser.

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 4435de7b-9377-4a42-bcf6-b4f51cdab720 34 fields · synced Jun 1, 2026