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Coulmed

FDA UDI

Class I (US FDA UDI)

by Coulmed Products Group Llc

Identity

Trade Name
Coulmed FDA UDI
Generic Name
Freestanding patient positioner, reusable FDA UDI
Device Name
Lithotomy Boot Pad, Small, Gel reusable boot stirrup pads (Allen Compatible), 2 Piece Set, 24" x 11-1/2" x 6" FDA UDI
Model / Reference
GP500 FDA UDI
Description
Lithotomy Boot Pad, Small, Gel reusable boot stirrup pads (Allen Compatible), 2 Piece Set, 24" x 11-1/2" x 6" FDA UDI

Identifiers

Catalog Number
GP500 FDA UDI
Primary DI / UDI-DI
10810087351639 FDA UDI
FDA Product Code
CCX FDA UDI
GMDN Term
Freestanding patient positioner, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6820 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Freestanding patient positioner, reusable

Coulmed by Coulmed Products Group Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Freestanding patient positioner, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d9c05280-02ba-4b12-b8f5-78b21c30b378 34 fields · synced Jun 6, 2026