FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Clarity™

DI: 00652221289537 · Model: 358-509 · 3M UNITEK CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
3M™ Clarity™
Primary DI
00652221289537
Version / Model
358-509
Catalog Number
358-509
Company Name
3M UNITEK CORPORATION
Labeler DUNS
008256356
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2020-06-29
Public Version
2
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
12a55d32-ff07-4326-a53b-bf3f5b21a94d

Device Description

3M™ Clarity™ Aligners Lost/Damage-Dual, 358-509

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NXC Aligner, Sequential

GMDN Terms

Code Name
44738 Orthodontic progressive aligner

Identifiers

Type ID
Primary 00652221289537
Unit of Use 80652221289533

Customer Contacts