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Precision Medical PM36PCCM

by Precision Medical Inc

Precision Medical PM36PCCM is a vacuum suction regulator/regulation set (FDA Class II; FDA product code KDP, Regulator, Vacuum) made by Precision Medical Inc, listed in FDA GUDID since 5 Jan 2026 (UDI-DI 00850027043814), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850027043814 UDI-DI Date5 Jan 2026ListedStatusListed 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  • Withdrawn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
Precision Medical
Generic name
Vacuum suction regulator/regulation set, general-purpose
Model / reference
PM36PCCM
Description
PM3600 SERIES,HF CONT VAC REG ,POLE CL,CALDERA MED
Primary DI / UDI-DI
00850027043814
FDA product code
KDP
GMDN term
Vacuum suction regulator/regulation set, general-purpose
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KDP (Regulator, Vacuum).

Other devices from Precision Medical Inc

See all devices from Precision Medical Inc →

Properties

  • Prescription use
  • Lot / batch number
  • Serial number
Other properties (12, all answered No)