FDA UDI In Commercial Distribution 🇺🇸 United States

Technomed Europe

DI: 08718375866863 · Model: TE/S50725-002 · Technomed Engineering B.V.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Technomed Europe
Primary DI
08718375866863
Version / Model
TE/S50725-002
Company Name
Technomed Engineering B.V.
Labeler DUNS
418415568
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-21
Public Version
2
Public Version Date
2023-06-15
Public Version Status
Update
Public Device Record Key
bfa0159d-fda9-4e36-a8c8-ad7655fab6cc

Device Description

Disposable Subdermal Needle Electrode corkscrew 2.0m twisted wire 12pairs

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GXZ Electrode, Needle
IKT Electrode, Needle, Diagnostic Electromyograph

GMDN Terms

Code Name
11441 Electromyographic needle electrode, single-use

Identifiers

Type ID
Package 08718375866870
Primary 08718375866863

Customer Contacts

Phone
+31434086868

Device Sizes

Type Value Unit Text
Outer Diameter 0.60 Millimeter
Length 2 Meter