FDA UDI In Commercial Distribution 🇺🇸 United States

Algovita®

DI: 00821329580376 · Model: 4900-USA · Greatbatch Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Algovita®
Primary DI
00821329580376
Version / Model
4900-USA
Catalog Number
4900
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
3
Public Version Date
2021-06-22
Public Version Status
Update
Public Device Record Key
4b5513fc-2485-4c77-b698-b700c1652be9

Device Description

Patient Magnet Kit

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
No
Has Lot/Batch Number
Yes
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
57996 Active implantable device control magnet

Identifiers

Type ID
Primary 00821329580376

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-35 – 55 Degrees Celsius