FDA UDI In Commercial Distribution 🇺🇸 United States

BIOTRONIK

DI: 04035479170301 · Model: Tunneler · BIOTRONIK SE & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BIOTRONIK
Primary DI
04035479170301
Version / Model
Tunneler
Catalog Number
457855
Company Name
BIOTRONIK SE & Co. KG
Labeler DUNS
315620229
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-04-06
Public Version
3
Public Version Date
2024-02-05
Public Version Status
Update
Public Device Record Key
0d19b7a7-1875-4c55-ad06-a662260cc5b9

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
LGW Stimulator, spinal-cord, totally implanted for pain relief

GMDN Terms

Code Name
46801 Subcutaneous tunneller, single-use

Identifiers

Type ID
Primary 04035479170301

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P210037 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
14 – 131 Degrees Fahrenheit