FDA UDI In Commercial Distribution 🇺🇸 United States

PRO-OPTIONS

DI: 07350111280031 · Model: 05053 · Pro-Options AB
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PRO-OPTIONS
Primary DI
07350111280031
Version / Model
05053
Company Name
Pro-Options AB
Labeler DUNS
554775309
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-01
Public Version
1
Public Version Date
2020-07-09
Public Version Status
New
Public Device Record Key
891343bb-3108-41ff-8333-0283f6da74c3

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
EIF Accessories, Retractor, Dental
EIG Retractor, All Types

GMDN Terms

Code Name
13380 Hand-held dental retractor

Identifiers

Type ID
Primary 07350111280031