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Dig-o-meter

FDA UDI

Class I (US FDA UDI)

by Therafin Corporation

Identity

Trade Name
Dig-o-meter FDA UDI
Generic Name
Finger/hand exerciser FDA UDI
Device Name
Dig-o-meter FDA UDI
Model / Reference
31900 FDA UDI
Description
Dig-o-meter FDA UDI

Identifiers

Catalog Number
31900 FDA UDI
Primary DI / UDI-DI
00840252911828 FDA UDI
FDA Product Code
IOD FDA UDI
GMDN Term
Finger/hand exerciser FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5350 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Finger/hand exerciser

Dig-o-meter by Therafin Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Finger/hand exerciser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 08620f1e-e883-4a24-b803-e3cf2951283e 35 fields · synced May 30, 2026