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Handheld Direct Drive Cable Trainer

FDA UDI

Class I (US FDA UDI)

by Beyond Power Inc.

Identity

Trade Name
Handheld Direct Drive Cable Trainer FDA UDI
Generic Name
Body/limb elastic exerciser FDA UDI
Device Name
Handheld Direct Drive Cable Trainer. FDA UDI
Model / Reference
HDDT-A1,Beyond Power Voltra I FDA UDI
Description
Handheld Direct Drive Cable Trainer. FDA UDI

Identifiers

Primary DI / UDI-DI
06977069493330 FDA UDI
FDA Product Code
BXB FDA UDI
GMDN Term
Body/limb elastic exerciser FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5380 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Body/limb elastic exerciser

Handheld Direct Drive Cable Trainer by Beyond Power Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Body/limb elastic exerciser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Beyond Power Inc.

Sources (1)

  • FDA UDI c6ac44c5-b38a-4430-ae2b-d1e405f60be9 33 fields · synced May 30, 2026