FDA UDI In Commercial Distribution 🇺🇸 United States

Algovita®

DI: 00821329580284 · Model: 4100-USA · Greatbatch Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Algovita®
Primary DI
00821329580284
Version / Model
4100-USA
Catalog Number
4100
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
4
Public Version Date
2020-07-07
Public Version Status
Update
Public Device Record Key
9c06f8b6-284f-44cd-ab7d-f154ec4e6b51

Device Description

Pocket Programmer (PoP)

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LGW Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

GMDN Terms

Code Name
61393 Multiple active implantable device programmer

Identifiers

Type ID
Primary 00821329580284

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal
Type
Storage Environment Humidity
Temperature Range
10 – 85 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius