FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00613994330079 · Model: 945DSE0005 · MEDTRONIC XOMED, INC.
Product Codes
6
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00613994330079
Version / Model
945DSE0005
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-08
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
8f3ea97b-8e6e-40e7-8e5f-ffa744504a71

Device Description

WIRE 945DSE0005 1.2M48IN ASSORTED LEAD

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
Yes
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
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE
GWE Stimulator, photic, evoked response
GWQ Full-montage Standard Electroencephalograph
GWJ STIMULATOR, AUDITORY, EVOKED RESPONSE
IYN System, imaging, pulsed doppler, ultrasonic
ITX Transducer, ultrasonic, diagnostic

GMDN Terms

Code Name
47714 Subdermal needle electrode

Identifiers

Type ID
Package 20613994330073
Primary 00613994330079

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K061639 000

Device Sizes

Type Value Unit Text
Length 1.2 Meter