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Vector 1

FDA UDI

Class I (US FDA UDI)

by Lantz Medical

Identity

Trade Name
Vector 1 FDA UDI
Generic Name
Hand/wrist continuous passive motion exerciser FDA UDI
Device Name
Exerciser to increase flexion and the extension range of motion of the joints of the second to the fifth fingers of the hand FDA UDI
Model / Reference
Vector 1 FDA UDI
Description
Exerciser to increase flexion and the extension range of motion of the joints of the second to the fifth fingers of the hand FDA UDI

Identifiers

Catalog Number
Vector 1 FDA UDI
Primary DI / UDI-DI
B770VEC0 FDA UDI
FDA Product Code
JFA FDA UDI
GMDN Term
Hand/wrist continuous passive motion exerciser FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5410 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

Yes

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

No

FDA UDI

Category: Hand/wrist continuous passive motion exerciser

Vector 1 by Lantz Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand/wrist continuous passive motion exerciser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Lantz Medical

Sources (1)

  • FDA UDI 62474b94-2c10-4f93-9aac-644b889c4388 34 fields · synced May 30, 2026