Cadwell 302882-000
Cadwell 302882-000 is a Class II device made by Technomed Engineering B.V., listed in FDA GUDID since 10 Dec 2025 (UDI-DI 08720791378530), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08720791378530 | Date10 Dec 2025 | StatusListed |
Official records
- AccessGUDID record 08720791378530
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Cadwell
- Generic name
- Subdermal needle electrode
- Model / reference
- 302882-000
- Primary DI / UDI-DI
- 08720791378530
- FDA product code
- IKT, GXZ
- GMDN term
- Subdermal needle electrode
- Device class
- Class II
- Regulation number
- 890.1385, 882.1350
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
- Size
- Needle Gauge — 27 GaugeOuter Diameter — 0.38 MillimeterLength — 13 Millimeter
Similar devices
Other devices filed under FDA product code IKT (Electrode, Needle, Diagnostic Electromyograph).
- TECA DISPOSABLE MONOPOLAR NEEDLE ELECTRODES by Medelec, Inc. D.B.A. Teca Corp.
- DISPOSABLE MONOPOLAR NEEDLE ELECTRODE, VAR MODELS by Chalgren Enterprises, Inc.
- DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12 by Dantec Medical, Inc.
- DISPOSABLE HYPODERMIC MONOPOLAR NEEDLE RECORDING ELECTRODE by Chalgren Enterprises, Inc.
- DISPOSABLE AND REUSABLE CONCENTRIC NEEDLES / DISPOSABLE AND REUSABLE MONOPOLAR NEEDLE by Bionen S.A.S.
- Myoject Luer Lock Needle Electrode by Natus Manufacturing Limited
- TECA ELITE DISPOSABLE CONCENTRIC NEEDLES by Carefusion 209, Inc.
- Allergan Botox Needle Electrode by Natus Manufacturing Limited
- MEB-5200 by NIHON KOHDEN AMERICA, INC.
- RHYTHMLINK DISPOSABLE MONOPOLAR EMG NEEDLE, MODEL TFDN26032252R by Rhythmlink International, LLC