FDA UDI Not in Commercial Distribution 🇺🇸 United States

ALLURE® MB

DI: D807101631041 · Model: 101-631-04 · DENTSPLY SIRONA ORTHODONTICS INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
ALLURE® MB
Primary DI
D807101631041
Version / Model
101-631-04
Catalog Number
101-631-04
Company Name
DENTSPLY SIRONA ORTHODONTICS INC.
Labeler DUNS
116903307
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2017-06-26
Public Version
6
Public Version Date
2024-03-01
Public Version Status
Update
Public Device Record Key
1ad31353-26d1-4cd0-96c0-ea7e6e5136c7
Distribution End Date
2021-01-15

Device Description

ALLURE® MB SEW .018 LOWER 3

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
No

Product Codes

Code Name
NJM Bracket, ceramic, orthodontic

GMDN Terms

Code Name
58937 Orthodontic bracket, ceramic

Identifiers

Type ID
Primary D807101631041
Unit of Use D807101631040

Customer Contacts