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Strap Pair 110

FDA UDI

Class I (US FDA UDI)

by Merivaara Oy

Identity

Trade Name
STRAP PAIR 110 FDA UDI
Generic Name
Limb/torso/head restraint, reusable FDA UDI
Device Name
Operating table accessory FDA UDI
Model / Reference
STRAP PAIR 110 FDA UDI
Description
Operating table accessory FDA UDI

Identifiers

Catalog Number
100000110 FDA UDI
Primary DI / UDI-DI
06438435001103 FDA UDI
FDA Product Code
FWZ FDA UDI
GMDN Term
Limb/torso/head restraint, 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Limb/torso/head restraint, reusable

Strap Pair 110 by Merivaara Oy — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Limb/torso/head restraint, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Merivaara Oy

Sources (1)

  • FDA UDI 44cbb283-a597-4617-8c90-c1fd663d4ff2 35 fields · synced May 30, 2026