← Back to catalogue

Camsource®

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref CSFHD01CC

by Joimax, Inc.

Identity

Trade Name
Camsource® FDA UDI
Generic Name
Endoscopic video image processing/light source system FDA UDI
Device Name
Camera Head Combo for Camsource® LED joimax® single cable technology, with function buttons EUDAMED
Camera Head Combo for Camsource® LED FDA UDI
Model / Reference
CSFHD01CC EUDAMEDFDA UDI
Description
Camera Head Combo for Camsource® LED FDA UDI

Identifiers

Catalog Number
CSFHD01CC FDA UDI
Primary DI / UDI-DI
04250337115229 EUDAMEDFDA UDI
Basic UDI-DI
42503371C+FUCCWG EUDAMED
Direct Marketing DI
04250337115229 EUDAMED
FDA Product Code
FWF FDA UDI
EMDN Code
Z12020402,Z12020405 EUDAMED
GMDN Term
Endoscopic video image processing/light source system FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4160 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic video image processing/light source system

Camsource® by Joimax, Inc. — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video image processing/light source system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Joimax, Inc.

Sources (2)

  • FDA UDI 70ba36cc-5cb2-4353-afd9-e50d6c98f039 37 fields · synced Jul 13, 2026
  • EUDAMED 2ca48449-4460-464f-8363-050395f2e658 61 fields · synced Jul 13, 2026