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universal motor handpiece

FDA UDI

Class I (US FDA UDI)

by Joimax, Inc.

Identity

Trade Name
universal motor handpiece FDA UDI
Generic Name
Arthroscopic shaver system, electrically-powered FDA UDI
Device Name
joimax® Universal Motor Handpiece FDA UDI
Model / Reference
JSDWD1500 FDA UDI
Description
joimax® Universal Motor Handpiece FDA UDI

Identifiers

Catalog Number
JSDWD1500 FDA UDI
Primary DI / UDI-DI
04250337112525 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Arthroscopic shaver system, electrically-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Arthroscopic shaver system, electrically-powered

universal motor handpiece by Joimax, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic shaver system, electrically-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Joimax, Inc.

Sources (1)

  • FDA UDI 07d07845-d8d4-46b6-9b18-ff147fbbe30c 35 fields · synced Jun 1, 2026