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Salvafix Memory PRO

FDA UDI

Class I (US FDA UDI)

by Medi Care System Slu

Identity

Trade Name
Salvafix Memory PRO FDA UDI
Generic Name
Limb/torso/head restraint, reusable FDA UDI
Device Name
Restraint Thorax Harness size M/L FDA UDI
Model / Reference
SVF3440 FDA UDI
Description
Restraint Thorax Harness size M/L FDA UDI

Identifiers

Primary DI / UDI-DI
08436035358342 FDA UDI
FDA Product Code
FMQ FDA UDI
GMDN Term
Limb/torso/head restraint, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6760 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Limb/torso/head restraint, reusable

Salvafix Memory PRO by Medi Care System Slu — 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
Medi Care System Slu

Sources (1)

  • FDA UDI 8d37b757-8ad8-44de-b637-e3e4b9711475 34 fields · synced Jun 8, 2026