FDA UDI In Commercial Distribution 🇺🇸 United States

Innervision, BioGlide®

DI: 00613994908476 · Model: 2120-925 · MEDTRONIC PS MEDICAL, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Innervision, BioGlide®
Primary DI
00613994908476
Version / Model
2120-925
Company Name
MEDTRONIC PS MEDICAL, INC.
Labeler DUNS
089055867
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-07-21
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
83bac517-defe-47a2-ab97-c7de97b5384d

Device Description

KIT 2120-925 INNER/ENDO SHUNT PLCMT BIO

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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GWG ENDOSCOPE, NEUROLOGICAL
HCA CATHETER, VENTRICULAR

GMDN Terms

Code Name
61491 Neuroscopic shunt placement kit

Identifiers

Type ID
Primary 00613994908476

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K940096 000

Device Sizes

Type Value Unit Text
Angle 0.0 degree
Length 15.5 Centimeter
Outer Diameter 1.1 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Fragile
Type
Special Storage Condition, Specify
Special Conditions
Keep Dry