Pressurizer
by Adler Ortho SpA 11 variants
Pressurizer (IZ03014) is a Class I device made by Adler Ortho SpA, listed in FDA GUDID since 7 Aug 2025 (UDI-DI 08053617183774), registry data as of 21 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08053617183774 | Date7 Aug 2025 | StatusListed |
Official records
- AccessGUDID record 08053617183774
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Orthopaedic cement compressor
- Model / Ref / Catalog
- Pressurizer, IZ03014
- Primary DI / UDI-DI
- 08053617183774
- FDA product code
- KIH
- GMDN term
- Orthopaedic cement compressor
- Device class
- Class I
- Regulation number
- 888.4200
- GUDID distribution status
- In Commercial Distribution
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- P.F.C. CEMENT PRESSURIZING SYSTEM by Johnson & Johnson Professionals, Inc.
- 0606100000 0606-100-000 by Stryker Corp.
- BONE CEMENT APPLICATOR by Zimmer, Inc.