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CoJet™

FDA UDI

Class II (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name
CoJet™ FDA UDI
Generic Name
Denture reliner, hard FDA UDI
Device Name
3M™ ESPE™ Cojet™ Adhesive Repair And Pretreatment Prior To Cementation System Set, 68420 FDA UDI
Model / Reference
68420 FDA UDI
Description
3M™ ESPE™ Cojet™ Adhesive Repair And Pretreatment Prior To Cementation System Set, 68420 FDA UDI

Identifiers

Catalog Number
68420 FDA UDI
Primary DI / UDI-DI
04035077001649 FDA UDI
FDA Product Code
EBF FDA UDI
KLE FDA UDI
KOJ FDA UDI
GMDN Term
Denture reliner, hard FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3690 FDA UDI
872.3200 FDA UDI
872.6080 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Category: Dentine bonding agent/setDenture reliner, hardDental composite resin kit

CoJet™ by 3M Deutschland GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental composite resin kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3M Deutschland GmbH

Sources (1)

  • FDA UDI 9f4ea3ff-4e34-4c8b-ba41-86d561111dfc 35 fields · synced May 30, 2026