FDA UDI In Commercial Distribution 🇺🇸 United States

tomas®

DI: J011302013000 · Model: 302-013-00 · DENTAURUM GmbH & Co.KG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
tomas®
Primary DI
J011302013000
Version / Model
302-013-00
Company Name
DENTAURUM GmbH & Co.KG
Labeler DUNS
315427286
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-15
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
96a81021-20b2-4be3-9948-3d3c090dd675

Device Description

tomas® anchorage system: tomas®-stop screw

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
OAT Implant, endosseous, orthodontic

GMDN Terms

Code Name
31759 Orthodontic tube

Identifiers

Type ID
Primary J011302013000
Unit of Use J011302013001

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
No special storage conditions required