Extension Arm 116

FDA UDI

Class I (US FDA UDI)

by Merivaara Oy

Identity

Trade Name: EXTENSION ARM 116 FDA UDI
Generic Name: Anaesthesia screen FDA UDI
Device Name: Operating table accessory FDA UDI
Model / Reference: EXTENSION ARM 116 FDA UDI
Description: Operating table accessory FDA UDI

Identifiers

Catalog Number: 100000116 FDA UDI
Primary DI / UDI-DI: 06438435001165 FDA UDI
FDA Product Code: FWZ FDA UDI
GMDN Term: Anaesthesia screen 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Anaesthesia screen

Extension Arm 116 by Merivaara Oy — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Anaesthesia screen.

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Schaerer Medical USA — Schaerer Medical Usa, Inc. · Class I
DRAPE ROD, REFURBISHED — Mizuho Orthopedic Systems, Inc. · Class I
Anesthesia screen — Skytron, LLC · Class I
Anaesthesia screen extension — Maquet, Inc. · Class I

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: Merivaara Oy

Sources (1)

FDA UDI 1d083a7c-8d48-4ec3-88f8-9428d9d74bb6 35 fields · synced May 29, 2026