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MIS Suction Adaptor 412-920

by Sontec Instruments, Inc.

MIS Suction Adaptor 412-920 is a Class I device made by Sontec Instruments, Inc., listed in FDA GUDID since 16 Oct 2025 (UDI-DI 00192896122260), 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 Number00192896122260 UDI-DI Date16 Oct 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  • Withdrawn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
MIS Suction Adaptor
Generic name
Endoscope flushing adaptor, reusable
Model / Ref / Catalog
412-920
Primary DI / UDI-DI
00192896122260
FDA product code
JZF
GMDN term
Endoscope flushing adaptor, reusable
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Dry Heat Sterilization

Similar devices

Other devices filed under FDA product code JZF (TUBE, EAR SUCTION).

Other devices from Sontec Instruments, Inc.

See all devices from Sontec Instruments, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)