FDA UDI Not in Commercial Distribution 🇺🇸 United States

NA

DI: 07613327282245 · Model: 5140-522-610 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613327282245
Version / Model
5140-522-610
Catalog Number
5140-522-610
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
2023-08-01
Public Version Status
Update
Public Device Record Key
f5a6e47d-5572-4d5d-a209-5295eeae7dc1
Distribution End Date
2020-12-31

Device Description

Bipolar Micro Fork Probe, 45mm straight

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
61089 Nerve-locating system probe, single-use

Identifiers

Type ID
Package 37613327282246
Primary 07613327282245

Device Sizes

Type Value Unit Text
Length 45.0 Millimeter

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
30 – 85 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
4 – 35 Degrees Celsius