FDA UDI In Commercial Distribution 🇺🇸 United States

TruFlex

DI: 00190730021113 · Model: 2008-113 · ORTHO TECHNOLOGY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TruFlex
Primary DI
00190730021113
Version / Model
2008-113
Company Name
ORTHO TECHNOLOGY, INC.
Labeler DUNS
781772017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-05-03
Public Version
1
Public Version Date
2019-05-13
Public Version Status
New
Public Device Record Key
58dbd7a6-edca-46ec-9753-234a19c7ec16

Device Description

TruFlex Copper 35 Euro 017 x 017 Up 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
Yes
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
DZC WIRE, ORTHODONTIC

GMDN Terms

Code Name
41397 Orthodontic archwire

Identifiers

Type ID
Primary 00190730021113