FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 04250307604456 · Model: 535640 · inomed Medizintechnik GmbH
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
04250307604456
Version / Model
535640
Company Name
inomed Medizintechnik GmbH
Labeler DUNS
340782259
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-12
Public Version
1
Public Version Date
2023-10-20
Public Version Status
New
Public Device Record Key
a531a0ce-e8be-4efd-8041-e905b452b53c

Device Description

Spine Surgery Set for EMG Recording

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
ETN Stimulator, Nerve

GMDN Terms

Code Name
11441 Electromyographic needle electrode, single-use

Identifiers

Type ID
Primary 04250307604456