FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 05415067027177 · Model: DRG · ST. JUDE MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
05415067027177
Version / Model
DRG
Catalog Number
MN10550-50
Company Name
ST. JUDE MEDICAL, INC.
Labeler DUNS
149818952
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-21
Public Version
5
Public Version Date
2023-08-01
Public Version Status
Update
Public Device Record Key
79a44101-d6c2-4212-b32b-3ff2679907e0

Device Description

Lead Extension Kit

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
PMP Dorsal root ganglion stimulator for pain relief

GMDN Terms

Code Name
65308 Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension

Identifiers

Type ID
Primary 05415067027177

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P150004 005

Device Sizes

Type Value Unit Text
Length 50.0000 Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-10 – 50 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
-10 – 50 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
10 – 90 Percent (%) Relative Humidity