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Buck's Traction Boot

FDA UDI

Class I (US FDA UDI)

by Primo Inc

Identity

Trade Name
Buck's Traction Boot FDA UDI
Generic Name
Freestanding patient positioner, single-use FDA UDI
Device Name
Buck's Traction Boot FDA UDI
Model / Reference
BT01-12 FDA UDI
Description
Buck's Traction Boot FDA UDI

Identifiers

Catalog Number
BT01-12 FDA UDI
Primary DI / UDI-DI
00810006681567 FDA UDI
FDA Product Code
ILZ FDA UDI
GMDN Term
Freestanding patient positioner, single-use 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Freestanding patient positioner, single-use

Buck's Traction Boot by Primo Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding patient positioner, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Primo Inc

Sources (1)

  • FDA UDI 0d005f51-62b8-4a9a-a0fd-b6862175f2f9 34 fields · synced May 31, 2026