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Vitus

FDA UDI

Class I (US FDA UDI)

by H R Pharmaceuticals, Inc.

Identity

Trade Name
Vitus FDA UDI
Generic Name
Ostomy odour-absorbent/deodorizer FDA UDI
Device Name
Vitus Lubricating Deodorant Disc Cap Bottle FDA UDI
Model / Reference
580 FDA UDI
Description
Vitus Lubricating Deodorant Disc Cap Bottle FDA UDI

Identifiers

Catalog Number
580 FDA UDI
Primary DI / UDI-DI
00850025153058 FDA UDI
FDA Product Code
EZS FDA UDI
GMDN Term
Ostomy odour-absorbent/deodorizer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5900 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

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ostomy odour-absorbent/deodorizer

Vitus by H R Pharmaceuticals, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ostomy odour-absorbent/deodorizer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
H R Pharmaceuticals, Inc.

Sources (1)

  • FDA UDI 865111ad-c95f-4a0c-903d-0c0139708afc 35 fields · synced Jun 6, 2026