Monoject

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name: Monoject FDA UDI
Generic Name: Test tube/reservoir cap FDA UDI
Device Name: Bouchon encliquete pour tubes de 16 mm,Yellow FDA UDI
Model / Reference: 1270019404 FDA UDI
Description: Bouchon encliquete pour tubes de 16 mm,Yellow FDA UDI

Identifiers

Catalog Number: 1270019404 FDA UDI
Primary DI / UDI-DI: 20884527004253 FDA UDI
FDA Product Code: LXG FDA UDI
GMDN Term: Test tube/reservoir cap FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 862.2050 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Test tube/reservoir cap

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Cardinalhealth

Sources (1)

FDA UDI 86fab1be-bd57-4f5e-83a8-61c9c265547e 36 fields · synced Jun 1, 2026