← Back to catalogue

Working Tube with Handle, oblique 45°

EUDAMEDFDA UDI

Class I (EU MDR)

Ref WTS177503Ref WTS178503

by Joimax GmbH

Identity

Trade Name
Working Tube with Handle, oblique 45° EUDAMED
Working sleeve FDA UDI
Generic Name
Endoscope sheath, reusable FDA UDI
Device Name
Working Tube with Handle, oblique 45° EUDAMEDFDA UDI
Working Tube Chisel EUDAMED
Model / Reference
WTS177503 EUDAMEDFDA UDI
WTS178503 EUDAMED
Description
Working Tube with Handle, oblique 45° FDA UDI

Identifiers

Catalog Number
WTS177503 FDA UDI
Primary DI / UDI-DI
04250337101826 EUDAMEDFDA UDI
04250337119203 EUDAMED
Basic UDI-DI
B-04250337101826 EUDAMED
42503371WOTUTUBY9 EUDAMED
Direct Marketing DI
04250337119203 EUDAMED
FDA Product Code
FZX FDA UDI
EMDN Code
L1199 NEUROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Endoscope sheath, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Working Tube with Handle, oblique 45° by Joimax GmbH — Class I — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Joimax GmbH
EUDAMED SRN
DE-MF-000009201

Sources (4)

  • EUDAMED 6a9eb3b2-0b79-45ff-8677-3182631dfe08 61 fields · synced Jul 28, 2026
  • EUDAMED 7a5aec75-a276-46c6-8b2d-bcdbf7adcd7e 61 fields · synced May 19, 2026
  • FDA UDI 10ccff25-1f4f-4ee6-bda0-53628918a37b 36 fields · synced May 29, 2026
  • EUDAMED 585ac95f-90bb-49ca-ad59-869a4fa96b5c 61 fields · synced Jun 20, 2026