FDA UDI In Commercial Distribution 🇺🇸 United States

Mucopren

DI: E217281051 · Model: 28105 · Kettenbach GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Mucopren
Primary DI
E217281051
Version / Model
28105
Catalog Number
28105
Company Name
Kettenbach GmbH & Co. KG
Labeler DUNS
316803246
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
4
Public Version Date
2018-08-09
Public Version Status
Update
Public Device Record Key
cd9129f6-edcc-4077-8667-5e11d872367e

Device Description

Mucopren Soft Basic Set

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
EBI Resin, Denture, Relining, Repairing, Rebasing

GMDN Terms

Code Name
34770 Denture reliner, elastic, long-term

Identifiers

Type ID
Primary E217281051

Customer Contacts

Phone
+4927747050

Premarket Submissions

Submission Number Supplement Number
K983357 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 25 Degrees Celsius