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Plum

FDA UDI

Class II (US FDA UDI)

by Icu Medical Fleet Services, Llc

Identity

Trade Name
Plum FDA UDI
Generic Name
Basic intravenous administration set, noninvasive FDA UDI
Device Name
Primary PLUM MICRODRIP Set CLAVE Secondary Port, Backcheck Valve, CLAVE Y-Site, Secure Lock, 104 Inch (previously Hospira product) FDA UDI
Model / Reference
1973201 FDA UDI
Description
Primary PLUM MICRODRIP Set CLAVE Secondary Port, Backcheck Valve, CLAVE Y-Site, Secure Lock, 104 Inch (previously Hospira product) FDA UDI

Identifiers

Catalog Number
1973201 FDA UDI
Primary DI / UDI-DI
10887787003434 FDA UDI
510(k) Number
K141789 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

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

Dimensions & Sizes

Size
Length — 104 Inch FDA UDI

Category: Basic intravenous administration set, noninvasive

Plum by Icu Medical Fleet Services, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic intravenous administration set, noninvasive.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4037d43b-bf62-4992-98d9-7256b3e5712d 38 fields · synced Jun 8, 2026