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VersaCare Patient Helper

FDA UDI

Class I (US FDA UDI)

by Zimmer Orthopaedic Surgical Products

Identity

Trade Name
VersaCare Patient Helper FDA UDI
Generic Name
Bed traction frame FDA UDI
Device Name
VersaCare Patient Helper Adapter for Hill-Rom VersaCare Bed FDA UDI
Model / Reference
00-2700-965-03 FDA UDI
Description
VersaCare Patient Helper Adapter for Hill-Rom VersaCare Bed FDA UDI

Identifiers

Catalog Number
00-2700-965-03 FDA UDI
Primary DI / UDI-DI
00889024373600 FDA UDI
FDA Product Code
HST FDA UDI
GMDN Term
Bed traction frame FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.5850 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Bed traction frame

VersaCare Patient Helper by Zimmer Orthopaedic Surgical Products — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bed traction frame.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c93ad3d4-455d-405a-91ce-f58b18a76e3a 35 fields · synced May 30, 2026