FDA UDI In Commercial Distribution 🇺🇸 United States

TalisMann Implant Kit

DI: 00816986020549 · Model: TM-1000 · BIOVENTUS LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
TalisMann Implant Kit
Primary DI
00816986020549
Version / Model
TM-1000
Company Name
BIOVENTUS LLC
Labeler DUNS
078450878
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-01
Public Version
2
Public Version Date
2026-03-27
Public Version Status
Update
Public Device Record Key
13af7784-c8ef-4698-a920-c1d170346e3f

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)

GMDN Terms

Code Name
65531 Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wireless connection

Identifiers

Type ID
Primary 00816986020549

Customer Contacts

Phone
888-453-2136

Premarket Submissions

Submission Number Supplement Number
K243678 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 55 Degrees Celsius