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Wolf-Pak

FDA UDI

Class II (US FDA UDI)

by Ndc Homecare Llc

Identity

Trade Name
Wolf-Pak FDA UDI
Generic Name
Basic intravenous administration set, noninvasive FDA UDI
Device Name
IV SET 20D 92" FLO REG Y 50/CS FDA UDI
Model / Reference
RF5000 FDA UDI
Description
IV SET 20D 92" FLO REG Y 50/CS FDA UDI

Identifiers

Catalog Number
RF5000 FDA UDI
Primary DI / UDI-DI
00857800006011 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Basic intravenous administration set, noninvasive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

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: Basic intravenous administration set, noninvasive

Wolf-Pak by Ndc Homecare Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic intravenous administration set, noninvasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ndc Homecare Llc

Sources (1)

  • FDA UDI aaca16f5-023e-4a65-8e83-75456543f48b 34 fields · synced May 30, 2026