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Shrill®

FDA UDI

Class I (US FDA UDI)

by Joimax, Inc.

Identity

Trade Name
Shrill® FDA UDI
Generic Name
Arthroscopic shaver system, electrically-powered FDA UDI
Device Name
joimax® Shrill® Deflector Shaft Kit 2, WL 320 mm FDA UDI
Model / Reference
JSBDSK FDA UDI
Description
joimax® Shrill® Deflector Shaft Kit 2, WL 320 mm FDA UDI

Identifiers

Catalog Number
JSBDSK FDA UDI
Primary DI / UDI-DI
04250337115939 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

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Arthroscopic shaver system, electrically-powered

Shrill® 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 7ec00184-b7df-4914-a1d5-f9b667fd4c05 36 fields · synced May 30, 2026