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CESSYS® Dorsal FHD Laminoscope (4.7 WCh), combo

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref LS7347068C

by Joimax GmbH

Identity

Trade Name
CESSYS® Dorsal FHD Laminoscope (4.7 WCh), combo EUDAMED
CESSYS® FDA UDI
Generic Name
Spinal endoscopic-access system FDA UDI
Device Name
CESSYS® Dorsal FHD Laminoscope (4.7 WCh), combo EUDAMEDFDA UDI
TESSYS® FHD Foraminoscope thoracic (3.1 WCh), Combo EUDAMED
Model / Reference
LS7347068C EUDAMEDFDA UDI
Description
CESSYS® Dorsal FHD Laminoscope (4.7 WCh), combo FDA UDI

Identifiers

Primary DI / UDI-DI
04250337114697 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337114697 EUDAMED
42503371ENSCFORG9 EUDAMED
Direct Marketing DI
04250337114697 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
Portugal EUDAMED
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

CESSYS® Dorsal FHD Laminoscope (4.7 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

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Manufacturer

Manufacturer
Joimax GmbH
EUDAMED SRN
DE-MF-000009201

Sources (3)

  • EUDAMED 607f44f7-8900-4ef2-b574-05c645c31e75 61 fields · synced Jun 19, 2026
  • FDA UDI 5fd56f7d-b6dd-4ece-8b5b-a589c8052a6b 35 fields · synced May 29, 2026
  • EUDAMED 9215f1e8-ff93-43d6-bb3b-34daa1ef353d 61 fields · synced Jun 19, 2026