FDA UDI In Commercial Distribution 🇺🇸 United States

3M™

DI: 00652221153593 · Model: 504-202 · 3M UNITEK CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
3M™
Primary DI
00652221153593
Version / Model
504-202
Catalog Number
504-202
Company Name
3M UNITEK CORPORATION
Labeler DUNS
008256356
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
7a58a5d2-2112-4e44-ad18-5891eb57b489

Device Description

Unitek(TM) TAD Cap Elastic Ring Ea

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
No

Product Codes

Code Name
DZE IMPLANT, ENDOSSEOUS, ROOT-FORM

GMDN Terms

Code Name
45251 Orthodontic appliance relief material

Identifiers

Type ID
Primary 00652221153593

Customer Contacts