FDA UDI In Commercial Distribution 🇺🇸 United States

3M™ Unitek™

DI: 00652221110329 · Model: 811-001 · 3M UNITEK CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
3M™ Unitek™
Primary DI
00652221110329
Version / Model
811-001
Catalog Number
811-001
Company Name
3M UNITEK CORPORATION
Labeler DUNS
008256356
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
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
4fce3e93-f669-49e1-8d41-f660025c7d5d

Device Description

3M™ Unitek™ Bracket Placement Instrument, 804-171, 1/Ea

Device Characteristics

Single Use
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
ECS PUSHER, BAND, ORTHODONTIC

GMDN Terms

Code Name
31801 Orthodontic metal band pusher

Identifiers

Type ID
Primary 00652221110329

Customer Contacts