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IV Administration Set Needless

FDA UDI

Class II (US FDA UDI)

by Geri-Gentle Corporation

Identity

Trade Name
IV Administration Set Needless FDA UDI
Generic Name
Basic intravenous administration set, noninvasive FDA UDI
Device Name
IV Administration Set Needless FDA UDI
Model / Reference
11222 FDA UDI
Description
IV Administration Set Needless FDA UDI

Identifiers

Primary DI / UDI-DI
00369771001259 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

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Basic intravenous administration set, noninvasive

IV Administration Set Needless by Geri-Gentle Corporation — 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
Geri-Gentle Corporation

Sources (1)

  • FDA UDI da287664-d04e-4877-bad2-1cf4d38eb39c 33 fields · synced Jun 8, 2026