FDA UDI In Commercial Distribution 🇺🇸 United States

OrthoFX

DI: 00860003321737 · Model: TB Retainer · ORTHOFX
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OrthoFX
Primary DI
00860003321737
Version / Model
TB Retainer
Company Name
ORTHOFX
Labeler DUNS
033755180
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-24
Public Version
3
Public Version Date
2021-08-05
Public Version Status
Update
Public Device Record Key
de636d3b-0f9c-4374-8c97-fb0086fc221e

Device Description

OrthoFX Retainer

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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
DYT Maintainer, Space Preformed, Orthodontic

GMDN Terms

Code Name
35310 Orthodontic retainer

Identifiers

Type ID
Primary 00860003321737

Customer Contacts

Phone
4159360006
Phone
9494137700