FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613327298024 · Model: 5140-534-620 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327298024
Version / Model
5140-534-620
Catalog Number
5140-534-620
Company Name
Stryker Leibinger GmbH & Co. KG
Labeler DUNS
316153956
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-23
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
8941b259-34c3-471b-a01f-c442f1b9da88

Device Description

Paired Subdermal Electrode RD, 12x2.5mm

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE

GMDN Terms

Code Name
47714 Subdermal needle electrode

Identifiers

Type ID
Package 37613327298025
Primary 07613327298024

Device Sizes

Type Value Unit Text
Length 12.0 Millimeter
Device Size Text, specify Offset: 2.5 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
TRANSPORT: 10-90%, -20+50¿C
Type
Storage Environment Temperature
Temperature Range
4 – 35 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
30 – 85 Percent (%) Relative Humidity