FDA UDI In Commercial Distribution 🇺🇸 United States

Algovita®

DI: 00821329580482 · Model: 3101-60-USA · Greatbatch Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Algovita®
Primary DI
00821329580482
Version / Model
3101-60-USA
Catalog Number
3101-60
Company Name
Greatbatch Ltd
Labeler DUNS
968623467
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-12-01
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
08ca9668-fefa-4bc3-8b54-09cde194e288

Device Description

Paddle Lead Kit (2 X 6 Electrode Configuration)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
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
36007 Analgesic spinal cord electrical stimulation system

Identifiers

Type ID
Primary 00821329580482

Device Sizes

Type Value Unit Text
Length 60 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-10 – 55 Degrees Celsius