Skip to content

Cadwell 302907-000

by Technomed Engineering B.V.

Cadwell 302907-000 is a Class II device made by Technomed Engineering B.V., listed in FDA GUDID since 26 May 2025 (UDI-DI 08720791377670), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08720791377670 UDI-DI Date26 May 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Cadwell
Generic name
Nerve-locating system probe, single-use
Model / reference
302907-000
Primary DI / UDI-DI
08720791377670
FDA product code
GXZ
GMDN term
Nerve-locating system probe, single-use
Device class
Class II
Regulation number
882.1350
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Nerve-locating system probe, single-use

Similar devices in this category

Other devices filed under Nerve-locating system probe, single-use.

Other devices from Technomed Engineering B.V.

See all devices from Technomed Engineering B.V. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)