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Bone Resector, Bullet Tip

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref JSBBT243533

by Joimax GmbH

Identity

Trade Name
Bone Resector, Bullet Tip EUDAMED
bone resector FDA UDI
Generic Name
Arthroscopic shaver system blade, single-use FDA UDI
Device Name
Bone Resector, Bullet Tip EUDAMEDFDA UDI
Barrel Cutter, Barrel Tip, with distal protection EUDAMED
Model / Reference
JSBBT243533 EUDAMEDFDA UDI
Description
Bone Resector, Bullet Tip FDA UDI

Identifiers

Catalog Number
JSBBT243533 FDA UDI
Primary DI / UDI-DI
04250337115519 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337115519 EUDAMED
42503371DEFLRESAK EUDAMED
Direct Marketing DI
04250337115519 EUDAMED
FDA Product Code
HWE FDA UDI
EMDN Code
Z12130585 MOTORISED ORTHOPAEDIC SURGERY SYSTEM INSTRUMENTS - CONSUMABLES EUDAMED
GMDN Term
Arthroscopic shaver system blade, single-use 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

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Spinal shaver system blade

Bone Resector, Bullet Tip by Joimax GmbH — Class IIa — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Spinal shaver system blade.

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 e1289568-b1f0-440f-8cac-3e025f806acf 61 fields · synced Jul 16, 2026
  • FDA UDI f419fc56-36c2-4145-a651-ab0ed5f923fe 36 fields · synced May 30, 2026
  • EUDAMED 0f0935b8-3aa3-4f77-bd48-c09fc3611b3b 61 fields · synced Jun 18, 2026