FDA UDI Not in Commercial Distribution 🇺🇸 United States

Ascenda

DI: 00613994555618 · Model: 8782 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ascenda
Primary DI
00613994555618
Version / Model
8782
Company Name
MEDTRONIC, INC.
Labeler DUNS
796986144
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-27
Public Version
4
Public Version Date
2022-12-23
Public Version Status
Update
Public Device Record Key
cab29549-d314-48b2-adc8-88b9f7c34600
Distribution End Date
2022-10-25

Device Description

CATH 8782 ASCENDA SPINAL REV SHORT EMAN

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LKK PUMP, INFUSION, IMPLANTED, PROGRAMMABLE

GMDN Terms

Code Name
61797 Lumbar cerebrospinal fluid drainage catheterization kit

Identifiers

Type ID
Primary 00613994555618

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P860004 125

Device Sizes

Type Value Unit Text
Length 86.0 Centimeter

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-34 – 57 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
-30 – 135 Degrees Fahrenheit