FDA UDI In Commercial Distribution 🇺🇸 United States

Globus

DI: 08718375866979 · Model: 693.061S · Technomed Engineering B.V.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Globus
Primary DI
08718375866979
Version / Model
693.061S
Company Name
Technomed Engineering B.V.
Labeler DUNS
418415568
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-03-27
Public Version
5
Public Version Date
2025-02-17
Public Version Status
Update
Public Device Record Key
88e9e7bc-8bf0-4327-8b98-d92426c38dea

Device Description

K-wire Stimulation Lead, Sterile 1 pc

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
Yes
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
IKD Cable, Electrode

GMDN Terms

Code Name
35750 Analytical non-scalp cutaneous lead

Identifiers

Type ID
Primary 08718375866979
Package 08718375866986

Customer Contacts

Phone
+31434086868