FDA UDI Not in Commercial Distribution 🇺🇸 United States

OrthoFX

DI: 18600033217131 · Model: ZR1 · ORTHOFX
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OrthoFX
Primary DI
18600033217131
Version / Model
ZR1
Company Name
ORTHOFX
Labeler DUNS
033755180
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-11
Public Version
3
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
9a708af2-9bd3-4ae8-85fd-ae9915c7b18f
Distribution End Date
2020-11-24

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 18600033217131

Customer Contacts

Phone
4159360006