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Genosyl®

FDA UDI

Class I (US FDA UDI)

by Vero Biotech Inc.

Identity

Trade Name
GENOSYL® FDA UDI
Generic Name
Nitric oxide delivery unit, system-based FDA UDI
Device Name
GENOSYL DS Bunnell Tee Adapters FDA UDI
Model / Reference
602532 FDA UDI
Description
GENOSYL DS Bunnell Tee Adapters FDA UDI

Identifiers

Catalog Number
602532 FDA UDI
Primary DI / UDI-DI
00850000962187 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Nitric oxide delivery unit, system-based FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5975 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nitric oxide delivery unit, system-based

Genosyl® by Vero Biotech Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nitric oxide delivery unit, system-based.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vero Biotech Inc.

Sources (1)

  • FDA UDI 26ec7f9b-699b-40f8-89f7-82f01699833c 35 fields · synced May 30, 2026