FDA UDI In Commercial Distribution 🇺🇸 United States

Perseus

DI: 08052675960044 · Model: 20902503 · ORTHOKEY ITALIA SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Perseus
Primary DI
08052675960044
Version / Model
20902503
Catalog Number
20902503
Company Name
ORTHOKEY ITALIA SRL
Labeler DUNS
433594191
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-01-17
Public Version
1
Public Version Date
2022-01-25
Public Version Status
New
Public Device Record Key
ee0cd821-a7b0-4aa1-b4c4-ffcd5f172e70

Device Description

Perseus Tibial Cutting Guide L - 1.3 mm

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
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
OLO Orthopedic Stereotaxic Instrument

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 08052675960044

Customer Contacts

Phone
+39055354829

Premarket Submissions

Submission Number Supplement Number
K192653 000