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Mobi-tools Grip

FDA UDI

Class I (US FDA UDI)

by Medi Care System Slu

Identity

Trade Name
Mobi-tools Grip FDA UDI
Generic Name
Manual patient lifting belt/harness FDA UDI
Device Name
Flexible belt for patient transfer and mobilization FDA UDI
Model / Reference
TMT6512 FDA UDI
Description
Flexible belt for patient transfer and mobilization FDA UDI

Identifiers

Primary DI / UDI-DI
08436035352630 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Manual patient lifting belt/harness FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 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 Safe FDA UDI

Category: Manual patient lifting belt/harness

Mobi-tools Grip by Medi Care System Slu — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual patient lifting belt/harness.

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 2f3918c8-c6a6-4fe6-bab6-97b4a2ace178 34 fields · synced May 29, 2026