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Jamar

FDA UDI

Class I (US FDA UDI)

by Asp Global, LLC

Identity

Trade Name
JAMAR FDA UDI
Generic Name
Hand dynamometer/pinchmeter, mechanical FDA UDI
Device Name
Jamar Plus+ Hand Evaluation Kit FDA UDI
Model / Reference
081505130 FDA UDI
Description
Jamar Plus+ Hand Evaluation Kit FDA UDI

Identifiers

Primary DI / UDI-DI
00840216112698 FDA UDI
FDA Product Code
HRW FDA UDI
GMDN Term
Hand dynamometer/pinchmeter, mechanical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1250 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hand dynamometer/pinchmeter, mechanical

Jamar by Asp Global, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand dynamometer/pinchmeter, mechanical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Asp Global, LLC

Sources (1)

  • FDA UDI 1e04afbf-1768-40c9-8faf-1818147fbe01 33 fields · synced Jun 8, 2026