Eforto

FDA UDI

Class II (US FDA UDI)

by Uniweb

Identity

Trade Name: Eforto FDA UDI
Generic Name: Hand dynamometer/pinchmeter, electronic FDA UDI
Device Name: Eforto M1 Vigorimeter FDA UDI
Model / Reference: M1 Vigorimeter FDA UDI
Description: Eforto M1 Vigorimeter FDA UDI

Identifiers

Primary DI / UDI-DI: 05430004547006 FDA UDI
FDA Product Code: LBB FDA UDI
GMDN Term: Hand dynamometer/pinchmeter, electronic FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.1240 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hand dynamometer/pinchmeter, electronic

Eforto by Uniweb — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Uniweb

Sources (1)

FDA UDI c29c9051-4705-4fea-8b76-e5996a432210 33 fields · synced May 30, 2026