Lightweight leg plate

FDA UDI

Class I (US FDA UDI)

by Maquet, Inc.

Identity

Trade Name: Lightweight leg plate FDA UDI
Generic Name: Leg procedure positioner FDA UDI
Model / Reference: 118048B0 FDA UDI

Identifiers

Primary DI / UDI-DI: 04046768031951 FDA UDI
FDA Product Code: BWN FDA UDI
GMDN Term: Leg procedure positioner 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Leg procedure positioner

Lightweight leg plate by Maquet, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Maquet, Inc.

Sources (1)

FDA UDI 0485c842-a9e0-4ded-9821-052f1a926cf6 32 fields · synced Jun 6, 2026