Identity
- Trade Name
- Pressurizer FDA UDI
- Generic Name
- Orthopaedic cement compressor FDA UDI
- Device Name
- PANTHEON PRESSURIZER STEM 18 FDA UDI
- Model / Reference
- Pressurizer FDA UDI
- Description
- PANTHEON PRESSURIZER STEM 18 FDA UDI
Identifiers
- Catalog Number
- IZ03018 FDA UDI
- Primary DI / UDI-DI
- 08053617183798 FDA UDI
- FDA Product Code
- KIH FDA UDI
- GMDN Term
- Orthopaedic cement compressor FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4200 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Orthopaedic cement compressor
Pressurizer by Adler Ortho Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Orthopaedic cement compressor.
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- Titan™ — Ascension Orthopedics, Inc. · Class I
- Pressurizer — ADLER ORTHO SPA · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Adler Ortho Spa
Sources (1)
- FDA UDI ff8668f4-ef84-4fb4-b082-54dc64c6e8db 34 fields · synced Jun 8, 2026