FDA UDI In Commercial Distribution 🇺🇸 United States

Pantera Pro

DI: 07640130436992 · Model: 3.00/10/140 · Biotronik AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Pantera Pro
Primary DI
07640130436992
Version / Model
3.00/10/140
Catalog Number
393295
Company Name
Biotronik AG
Labeler DUNS
480862817
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-17
Public Version
4
Public Version Date
2019-10-07
Public Version Status
Update
Public Device Record Key
3feb04ef-f2de-429e-be9f-312a5b211554

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LOX Catheters, transluminal coronary angioplasty, percutaneous

GMDN Terms

Code Name
47732 Coronary angioplasty balloon catheter, basic

Identifiers

Type ID
Primary 07640130436992

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K160985 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 3 mm
Device Size Text, specify Usable Length: 140 cm
Device Size Text, specify Length: 10 mm

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight Keep dry