← Back to catalogue

TESSYS® XT Working Tube with Handle

EUDAMEDFDA UDI

Class I (EU MDR)

Ref WTS217500

by Joimax GmbH

Identity

Trade Name
TESSYS® XT Working Tube with Handle EUDAMED
TESSYS® FDA UDI
Generic Name
Endoscope sheath, reusable FDA UDI
Device Name
Working Tube Chisel EUDAMED
TESSYS® XT Working Tube with Handle EUDAMEDFDA UDI
Model / Reference
WTS217500 EUDAMEDFDA UDI
Description
TESSYS® XT Working Tube with Handle FDA UDI

Identifiers

Catalog Number
WTS217500 FDA UDI
Primary DI / UDI-DI
04250337101871 EUDAMEDFDA UDI
Basic UDI-DI
42503371WOTUTUBY9 EUDAMED
B-04250337101871 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

TESSYS® XT Working Tube with Handle by Joimax GmbH — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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 (3)

  • EUDAMED e89f13aa-1a07-4d12-bed7-eaf11e9ec492 61 fields · synced Jul 11, 2026
  • EUDAMED 30b8bb46-10b7-4599-ad9a-3b707ff03e63 61 fields · synced May 19, 2026
  • FDA UDI 8c6963a8-05fe-4f74-879c-faf980e9145e 36 fields · synced May 30, 2026