← Back to catalogue

Monoject

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Monoject FDA UDI
Generic Name
Medical tubing clip/clamp, temporary, non-calibrated, single-use FDA UDI
Device Name
Snap Cap for 13 mm Tubes,Green FDA UDI
Model / Reference
1270019503 FDA UDI
Description
Snap Cap for 13 mm Tubes,Green FDA UDI

Identifiers

Catalog Number
1270019503 FDA UDI
Primary DI / UDI-DI
20884527004307 FDA UDI
FDA Product Code
LXG FDA UDI
GMDN Term
Medical tubing clip/clamp, temporary, non-calibrated, single-use 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

No

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

Category: Medical tubing clip/clamp, temporary, non-calibrated, single-use

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

Similar devices

Also classified as Medical tubing clip/clamp, temporary, non-calibrated, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 87d8870c-14b2-425f-a252-e7f5732dd8bd 36 fields · synced May 30, 2026