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Renovar Advanced

FDA UDI

Class U (US FDA UDI)

by H R Pharmaceuticals, Inc.

Identity

Trade Name
Renovar Advanced FDA UDI
Generic Name
Non-antimicrobial wound irrigation solution, multiple solute FDA UDI
Device Name
Renovar Advanced Skin and Wound Cleanser 8oz Dispensing Cap Bottle FDA UDI
Model / Reference
60491 FDA UDI
Description
Renovar Advanced Skin and Wound Cleanser 8oz Dispensing Cap Bottle FDA UDI

Identifiers

Catalog Number
60491 FDA UDI
Primary DI / UDI-DI
00850025153904 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Non-antimicrobial wound irrigation solution, multiple solute FDA UDI

Classification

Device Class
U 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-antimicrobial wound irrigation solution, multiple solute

Renovar Advanced by H R Pharmaceuticals, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-antimicrobial wound irrigation solution, multiple solute.

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 d340a72d-df23-45cd-b79a-4cd11c53eb87 35 fields · synced Jun 6, 2026