← Back to catalogue

iLESSYS® FHD Laminoscope (3.7 WCh), combo

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref LS6342125C

by Joimax GmbH

Identity

Trade Name
iLESSYS® FHD Laminoscope (3.7 WCh), combo EUDAMED
iLESSYS® FDA UDI
Generic Name
Spinal endoscopic-access system FDA UDI
Device Name
iLESSYS® FHD Laminoscope (3.7 WCh), combo EUDAMED
TESSYS® FHD Foraminoscope thoracic (3.1 WCh), Combo EUDAMED
iLESSYS® HD Laminoscope (3.7 mm WCh), combo FDA UDI
Model / Reference
LS6342125C EUDAMEDFDA UDI
Description
iLESSYS® HD Laminoscope (3.7 mm WCh), combo FDA UDI

Identifiers

Primary DI / UDI-DI
04250337105756 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337105756 EUDAMED
42503371ENSCFORG9 EUDAMED
Direct Marketing DI
04250337105756 EUDAMED
510(k) Number
K051827 FDA UDI
FDA Product Code
HRX FDA UDI
EMDN Code
Z12021199 ORTHOPAEDIC ENDOSCOPY INSTRUMENTS - OTHER EUDAMED
GMDN Term
Spinal endoscopic-access system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
888.1100 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid endoscope obturator

iLESSYS® FHD Laminoscope (3.7 WCh), combo by Joimax GmbH — Class IIa — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscope obturator.

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 (3)

  • EUDAMED b03b56c6-bb57-45fa-8aa1-95b45f3b575b 61 fields · synced Jun 18, 2026
  • FDA UDI b75e6536-818b-41d5-ac1c-64d53c02f21e 35 fields · synced May 30, 2026
  • EUDAMED 3143d3e2-033a-4867-9307-8d809d58cf51 61 fields · synced Jun 18, 2026