FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Unitek™

DI: 00652221167729 · Model: 4582-305 · 3M UNITEK CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
3M™ Unitek™
Primary DI
00652221167729
Version / Model
4582-305
Catalog Number
4582-305
Company Name
3M UNITEK CORPORATION
Labeler DUNS
008256356
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
c599382b-a596-4d7f-9e22-3cd651e1edeb

Device Description

3M™ Unitek™ Beta Titanium Lateral Development Archwire 4582-305, .017x.025, R26, 10/Pk

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
Yes
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
DZC WIRE, ORTHODONTIC

GMDN Terms

Code Name
41397 Orthodontic archwire

Identifiers

Type ID
Unit of Use 80652221167725
Primary 00652221167729

Customer Contacts