FDA UDI In Commercial Distribution 🇺🇸 United States

CoJet™

DI: J001702011129120 · Model: 68420 · 3M Deutschland GmbH
Product Codes
3
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CoJet™
Primary DI
J001702011129120
Version / Model
68420
Catalog Number
68420
Company Name
3M Deutschland GmbH
Labeler DUNS
315731711
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2024-02-16
Public Version Status
Update
Public Device Record Key
e4507608-f005-433d-8cb0-127c98aff8b0

Device Description

3M™ ESPE™ Cojet™ Adhesive Repair And Pretreatment Prior To Cementation System Set, 68420

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EBF MATERIAL, TOOTH SHADE, RESIN
KOJ AIRBRUSH
KLE AGENT, TOOTH BONDING, RESIN

GMDN Terms

Code Name
17609 Denture reliner, hard
34782 Dentine bonding agent/set
62477 Dental composite resin kit

Identifiers

Type ID
Primary J001702011129120

Customer Contacts