FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 04250307607303 · Model: 504106 · inomed Medizintechnik GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
04250307607303
Version / Model
504106
Company Name
inomed Medizintechnik GmbH
Labeler DUNS
340782259
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-23
Public Version
1
Public Version Date
2023-01-31
Public Version Status
New
Public Device Record Key
fc5e4a10-a8a6-4cba-b36c-353679c02f83

Device Description

ISIS Xpress empty case

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
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
36081 Nerve-function monitor

Identifiers

Type ID
Primary 04250307607303