FDA UDI In Commercial Distribution 🇺🇸 United States

VBR

DI: 07640173166016 · Model: P15.010.351 · coLigne AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VBR
Primary DI
07640173166016
Version / Model
P15.010.351
Company Name
coLigne AG
Labeler DUNS
482467792
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-15
Public Version
4
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
5149578b-ff2b-4145-b20d-4785454e3b42

Device Description

ostapek cage

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

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

Product Codes

Code Name
MQP Spinal Vertebral Body Replacement Device

GMDN Terms

Code Name
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary 07640173166016

Customer Contacts

Phone
+41433438000

Premarket Submissions

Submission Number Supplement Number
K072326 000