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Pressurizer

FDA UDI

Class I (US FDA UDI)

by Adler Ortho Spa

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

Similar devices

Also classified as Orthopaedic cement compressor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Adler Ortho Spa

Sources (1)

  • FDA UDI ff8668f4-ef84-4fb4-b082-54dc64c6e8db 34 fields · synced Jun 8, 2026