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Technomed Europe TE/B50700-001

by Technomed Engineering B.V.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08720791378059 UDI-DI Date29 Apr 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Technomed Europe
Generic Name
Electromyographic needle electrode, single-use
Model / Reference
TE/B50700-001
Primary DI / UDI-DI
08720791378059
FDA Product Code
GXZ, IKT
GMDN Term
Electromyographic needle electrode, single-use
Device Class
Class II
Regulation Number
882.1350, 890.1385
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Technomed Engineering B.V.

See all devices from Technomed Engineering B.V. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No