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Shrill® Deflector Shaft 2, WL= 320mm, reusable

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref JSBDS3522

by Joimax GmbH

Identity

Trade Name
Shrill® Deflector Shaft 2, WL= 320mm, reusable EUDAMED
deflector schaft FDA UDI
Generic Name
Arthroscopic shaver system, electrically-powered FDA UDI
Device Name
Shrill® Deflector Shaft 2, WL= 320mm, reusable EUDAMEDFDA UDI
Shrill® Deflector Shaft 2, WL= 265mm, reusable EUDAMED
Model / Reference
JSBDS3522 EUDAMEDFDA UDI
Description
Shrill® Deflector Shaft 2, WL= 320mm, reusable FDA UDI

Identifiers

Catalog Number
JSBDS3522 FDA UDI
Primary DI / UDI-DI
04250337108252 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337108252 EUDAMED
42503371DEFLSHA9V EUDAMED
Direct Marketing DI
04250337108252 EUDAMED
FDA Product Code
HWE FDA UDI
EMDN Code
L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Arthroscopic shaver system, electrically-powered FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMEDEUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

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

Shrill® Deflector Shaft 2, WL= 320mm, reusable by Joimax GmbH — Class IIa — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Joimax GmbH
EUDAMED SRN
DE-MF-000009201

Sources (3)

  • EUDAMED de662c8c-b584-4f59-b908-652884f055d4 61 fields · synced Jul 25, 2026
  • FDA UDI 9848cd45-a13d-448b-940c-86fb1de2fb2d 36 fields · synced May 30, 2026
  • EUDAMED 371a6f53-c8aa-4cd2-82ea-397314cb1885 61 fields · synced Jul 25, 2026