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Monoject

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Monoject FDA UDI
Generic Name
Medication transfer needle, non-filtering/non-vented FDA UDI
Device Name
Medication Transfer Needle FDA UDI
Model / Reference
8881204021 FDA UDI
Description
Medication Transfer Needle FDA UDI

Identifiers

Catalog Number
8881204021 FDA UDI
Primary DI / UDI-DI
10884521151260 FDA UDI
FDA Product Code
GAA FDA UDI
GMDN Term
Medication transfer needle, non-filtering/non-vented FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 1 Inch FDA UDI

Category: Medication transfer needle, non-filtering/non-vented

Monoject by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medication transfer needle, non-filtering/non-vented.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 0963d4ec-2f9a-40c4-8ee6-6abbe734b613 37 fields · synced May 30, 2026