FDA UDI In Commercial Distribution 🇺🇸 United States

OrthoMedFlex

DI: M7161013190 · Model: 101-319 · ORTHOMEDFLEX LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OrthoMedFlex
Primary DI
M7161013190
Version / Model
101-319
Catalog Number
101-319
Company Name
ORTHOMEDFLEX LLC
Labeler DUNS
034442726
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-29
Public Version
3
Public Version Date
2023-01-20
Public Version Status
Update
Public Device Record Key
0c813727-abda-468e-8a1b-12b3bcfce15b

Device Description

Offset Cup Impactor

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
Yes
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
HWA Impactor

GMDN Terms

Code Name
32856 Orthopaedic implant impactor, reusable

Identifiers

Type ID
Primary M7161013190

Customer Contacts

Phone
8446633539