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Belt Qc Ambulation

FDA UDI

Class I (US FDA UDI)

by AliMed, LLC

Identity

Trade Name
BELT QC AMBULATION FDA UDI
Generic Name
Movement-resistance gait rehabilitation device FDA UDI
Model / Reference
77905 FDA UDI

Identifiers

Catalog Number
2970010245 FDA UDI
Primary DI / UDI-DI
00733657229271 FDA UDI
FDA Product Code
IKX FDA UDI
GMDN Term
Movement-resistance gait rehabilitation device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 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

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Movement-resistance gait rehabilitation device

Belt Qc Ambulation by AliMed, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Movement-resistance gait rehabilitation device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AliMed, LLC

Sources (1)

  • FDA UDI 5b832e51-dd95-481f-b245-3b27d6efbdc3 34 fields · synced Jun 9, 2026