FDA UDI In Commercial Distribution 🇺🇸 United States

OrthoMedFlex

DI: M71610120301 · Model: 101-203-01 · ORTHOMEDFLEX LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OrthoMedFlex
Primary DI
M71610120301
Version / Model
101-203-01
Catalog Number
10120301
Company Name
ORTHOMEDFLEX LLC
Labeler DUNS
034442726
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-27
Public Version
3
Public Version Date
2018-08-09
Public Version Status
Update
Public Device Record Key
e231b641-de4b-4c24-b418-cd87c5121ae5

Device Description

T-Handle Instrument

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HXX Screwdriver

GMDN Terms

Code Name
47829 Surgical instrument handle, non-torque-limiting

Identifiers

Type ID
Primary M71610120301

Customer Contacts