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Video TWISTER

FDA UDI

Class I (US FDA UDI)

by Joimax, Inc.

Identity

Trade Name
Video TWISTER FDA UDI
Generic Name
Endoscopic video image processing unit FDA UDI
Device Name
Footswitch with 2 pedals for joimax® Video TWISTER FDA UDI
Model / Reference
JVTBFS001 FDA UDI
Description
Footswitch with 2 pedals for joimax® Video TWISTER FDA UDI

Identifiers

Catalog Number
JVTBFS001 FDA UDI
Primary DI / UDI-DI
04250337100836 FDA UDI
FDA Product Code
FWF FDA UDI
GMDN Term
Endoscopic video image processing unit 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

Category: Endoscopic video image processing unit

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

Similar devices

Also classified as Endoscopic video image processing unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Joimax, Inc.

Sources (1)

  • FDA UDI e2bbfdab-e3a4-46ae-823a-dae88c69c5f1 35 fields · synced May 30, 2026