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A-dec 77.1705.00

by A-Dec, Inc.

A-dec 77.1705.00 is a Class I device made by A-Dec, Inc., listed in FDA GUDID since 27 Oct 2022 (UDI-DI 10194665002893), 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 Number10194665002893 UDI-DI Date27 Oct 2022ListedStatusListed 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  • Withdrawn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
A-dec
Generic name
Dental suction system
Model / Ref / Catalog
77.1705.00
Primary DI / UDI-DI
10194665002893
FDA product code
EHZ
GMDN term
Dental suction system
Device class
Class I
Regulation number
872.6640
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental suction system

Similar devices in this category

Other devices filed under Dental suction system.

Other devices from A-Dec, Inc.

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  • A-dec 54.1074.01

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  • A-dec 54.1073.01

    Class I

See all devices from A-Dec, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Manufacturing date
Other properties (12, all answered No)