FDA UDI In Commercial Distribution 🇺🇸 United States

Ketac™ Universal Aplicap™

DI: 04035077009836 · Model: 61085 · 3M Deutschland GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ketac™ Universal Aplicap™
Primary DI
04035077009836
Version / Model
61085
Catalog Number
61085
Company Name
3M Deutschland GmbH
Labeler DUNS
315731711
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-04
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
00dd5557-195b-471f-a107-5ae7a7ec31fd

Device Description

3M™ ESPE™ Ketac™ Universal Aplicap™ Refill Assorted, 50 Capsules, 61085

Device Characteristics

Single Use
Yes
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
EMA CEMENT, DENTAL

GMDN Terms

Code Name
16704 Glass ionomer dental cement

Identifiers

Type ID
Primary 04035077009836

Customer Contacts