FDA UDI In Commercial Distribution 🇺🇸 United States

OrthoMedFlex

DI: M7161111962630 · Model: 111196263 · ORTHOMEDFLEX LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OrthoMedFlex
Primary DI
M7161111962630
Version / Model
111196263
Catalog Number
111-19-6263
Company Name
ORTHOMEDFLEX LLC
Labeler DUNS
034442726
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-16
Public Version
4
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
aa7ebb1b-a41a-42f6-b3fd-cc9af5f16c00

Device Description

Orion (Remedy) Trial Neck, High Offset, Size 4-5

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
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
58481 Femoral stem prosthesis trial

Identifiers

Type ID
Primary M7161111962630