FDA UDI In Commercial Distribution 🇺🇸 United States

Cadwell

DI: 08720791375911 · Model: 302881-000 · Technomed Engineering B.V.
Product Codes
3
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Cadwell
Primary DI
08720791375911
Version / Model
302881-000
Company Name
Technomed Engineering B.V.
Labeler DUNS
418415568
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-03-12
Public Version
1
Public Version Date
2025-03-20
Public Version Status
New
Public Device Record Key
ad3b30cc-bd82-4869-b375-7e15fa1d5a20

Device Description

The kit consists of: • 1x Ground Electrode 40x50mm (302299-000-078), • 2x Twisted Pair Surface Electrode 20x25mm disk (302880-000), • White Subdermal Needle (302864-000), and • 8x Twisted Subdermal Needles (white or black+ red, blue, purple, orange) (302868-000).

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

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

GMDN Terms

Code Name
47714 Subdermal needle electrode
61020 Analytical non-scalp cutaneous electrode

Identifiers

Type ID
Primary 08720791375911