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FHD Nucleoscope [1, 9 mm OD] Ocular

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref PS1909132O

by Joimax GmbH

Identity

Trade Name
FHD Nucleoscope [1,9 mm OD] Ocular EUDAMED
FHD Nucleoscope (1,9 mm OD) Ocular EUDAMED
joimax® FDA UDI
Generic Name
Spinal endoscopic-access system FDA UDI
Device Name
FHD Nucleoscope [1,9 mm OD] Ocular EUDAMED
joimax® Arthroscope Combo EUDAMED
HD Nucleoscope [1.9 mm OD] Ocular FDA UDI
Model / Reference
PS1909132O EUDAMEDFDA UDI
Description
HD Nucleoscope [1.9 mm OD] Ocular FDA UDI

Identifiers

Primary DI / UDI-DI
04250337109679 EUDAMEDFDA UDI
Basic UDI-DI
B-04250337109679 EUDAMED
42503371ENSCARTFV EUDAMED
Direct Marketing DI
04250337109679 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

FHD Nucleoscope [1, 9 mm OD] Ocular 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 ad369d3b-0185-4b88-93da-73e2fa64e347 61 fields · synced Jul 16, 2026
  • FDA UDI eef88824-c605-4e79-b8c5-455b1cc8e18c 35 fields · synced May 30, 2026
  • EUDAMED 7faa8dac-e76c-4713-b6ed-7db137f00b6b 61 fields · synced Jul 16, 2026