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video lens

FDA UDI

Class I (US FDA UDI)

by Joimax, Inc.

Identity

Trade Name
video lens FDA UDI
Generic Name
Fibreoptic light cable FDA UDI
Device Name
joimax® Video Lens, zoomable FDA UDI
Model / Reference
CSFHD01COVZ FDA UDI
Description
joimax® Video Lens, zoomable FDA UDI

Identifiers

Catalog Number
CSFHD01COVZ FDA UDI
Primary DI / UDI-DI
04250337117384 FDA UDI
FDA Product Code
FWF FDA UDI
GMDN Term
Fibreoptic light cable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fibreoptic light cable

video lens by Joimax, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic light cable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Joimax, Inc.

Sources (1)

  • FDA UDI df2a37af-2e32-411f-a8d4-7f5e07b4c7d5 37 fields · synced May 30, 2026