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NOVO Health Services, LLC

FDA UDI

Class I (US FDA UDI)

by Novo Health Services, Llc

Identity

Trade Name
NOVO Health Services, LLC FDA UDI
Generic Name
Emesis bowl, reusable FDA UDI
Device Name
Bowl, Eye 900cc FDA UDI
Model / Reference
124122 FDA UDI
Description
Bowl, Eye 900cc FDA UDI

Identifiers

Catalog Number
124122 FDA UDI
Primary DI / UDI-DI
00812564032720 FDA UDI
FDA Product Code
FNY FDA UDI
GMDN Term
Emesis bowl, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6730 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Category: Emesis bowl, reusable

NOVO Health Services, LLC by Novo Health Services, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Emesis bowl, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 01cf0c87-21fc-4522-a8ba-cebd1d45b694 35 fields · synced Jun 6, 2026