FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 07613327301229 · Model: 5140-540-425 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327301229
Version / Model
5140-540-425
Catalog Number
5140-540-425
Company Name
Stryker Leibinger GmbH & Co. KG
Labeler DUNS
316153956
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-22
Public Version
3
Public Version Date
2023-07-28
Public Version Status
Update
Public Device Record Key
dc356369-9dbc-4fb2-bf42-7eaff13bc2e2
Distribution End Date
2020-12-31

Device Description

Electrode Connection Box, 4 Channel

Device Characteristics

Single Use
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE

GMDN Terms

Code Name
35723 Nerve-locating system

Identifiers

Type ID
Primary 07613327301229