← Back to catalogue

Hand and arm positioning table

FDA UDI

Class I (US FDA UDI)

by Maquet, Inc.

Identity

Trade Name
Hand and arm positioning table FDA UDI
Generic Name
Arm procedure positioner, reusable FDA UDI
Model / Reference
44029002 FDA UDI

Identifiers

Primary DI / UDI-DI
04046768001008 FDA UDI
FDA Product Code
BWN FDA UDI
GMDN Term
Arm procedure positioner, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4950 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Arm procedure positioner, reusable

Hand and arm positioning table by Maquet, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arm procedure positioner, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Maquet, Inc.

Sources (1)

  • FDA UDI 03d44502-6cfa-47f7-ae50-5ca89cf93e5e 32 fields · synced Jun 6, 2026