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Novo Vivo

FDA UDI

Class I (US FDA UDI)

by Genesis Industries, Incorporated

Identity

Trade Name
Novo Vivo FDA UDI
Generic Name
Assisted reproduction transfer catheter trial FDA UDI
Device Name
Novo Vivo Suction Catheter FDA UDI
Model / Reference
05100 FDA UDI
Description
Novo Vivo Suction Catheter FDA UDI

Identifiers

Catalog Number
05100 FDA UDI
Primary DI / UDI-DI
00736239051000 FDA UDI
FDA Product Code
GBS FDA UDI
GMDN Term
Assisted reproduction transfer catheter trial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assisted reproduction transfer catheter trial

Novo Vivo by Genesis Industries, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assisted reproduction transfer catheter trial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7ccb3e56-7449-4235-8c99-0a6f1c97f38b 34 fields · synced May 31, 2026