FDA UDI In Commercial Distribution 🇺🇸 United States

ORTHOMAP

DI: 07613252450108 · Model: 6007-616-100 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ORTHOMAP
Primary DI
07613252450108
Version / Model
6007-616-100
Catalog Number
6007-616-100
Company Name
Stryker Leibinger GmbH & Co. KG
Labeler DUNS
316153956
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-12
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
19348d3e-25be-4b6e-b440-fbe52d940d1b

Device Description

ORTHOMAP¿ VERSATILE HIP 2.0 - UPGRADE

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
No
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
No

Product Codes

Code Name
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
42895 Robotic surgical navigation system application software

Identifiers

Type ID
Primary 07613252450108