Skip to content

Pressurizer

by Adler Ortho SpA 11 variants

Pressurizer (IZ03011) is a Class I device made by Adler Ortho SpA, listed in FDA GUDID since 7 Aug 2025 (UDI-DI 08053617183750), registry data as of 8 Jun 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 Jun 2026.

Regulatory status

as of registry sync 8 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08053617183750 UDI-DI Date7 Aug 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  • Withdrawn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

Generic name
Orthopaedic cement compressor
Model / Ref / Catalog
Pressurizer, IZ03011
Primary DI / UDI-DI
08053617183750
FDA product code
KIH
GMDN term
Orthopaedic cement compressor
Device class
Class I
Regulation number
888.4200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthopaedic cement compressor

Similar devices

Other devices filed under FDA product code KIH (Dispenser, Cement).

Other devices from Adler Ortho SpA

See all devices from Adler Ortho SpA →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)