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Magnetic Probe 2800-7480

by Sontec Instruments, Inc. 2 variants

Magnetic Probe 2800-7480 is a Class I device made by Sontec Instruments, Inc., listed in FDA GUDID since 7 Sep 2018 (UDI-DI 00192896070158), 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 Number00192896070158 UDI-DI Date7 Sep 2018ListedStatusListed 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  • Withdrawn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
Magnetic Probe
Generic name
Endoscopic surgical probe
Model / Ref / Catalog
2800-7480
Primary DI / UDI-DI
00192896070158
FDA product code
FGM
GMDN term
Endoscopic surgical probe
Device class
Class I
Regulation number
876.4730
GUDID distribution status
In Commercial Distribution
Size
Length — 13.75 Inch

Related devices

Category: Endoscopic surgical probe

Similar devices in this category

Other devices filed under Endoscopic surgical probe.

Other devices from Sontec Instruments, Inc.

See all devices from Sontec Instruments, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)