eudamed_udi
Primary ID: 00887761968073
PST 300 (UDI 00887761968073)
Manufactured by Baxter Medical Systems GmbH + Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PST 300 - Primary ID 00887761968073
Device Regulatory Overview
The PST 300 (Model/Catalog Number: 2072783) is a medical device manufactured by Baxter Medical Systems GmbH + Co. KG. This product is indexed under FDA Product Code / Category Classification Z12011202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2072783
- Product Code / EMDN
- Z12011202
- Device Name
- PST 300 Mobile Operating Table
- Database Sync Date
- 2026-08-09 16:29:20
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of PST 300?
The registered manufacturer of record for PST 300 is Baxter Medical Systems GmbH + Co. KG.
What is the Primary UDI-DI identifier for PST 300?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00887761968073.
What classification code is assigned to this device?
This device is registered under product classification code Z12011202.
Similar Classification Devices (Z12011202)
Other Devices by Baxter Medical Systems GmbH + Co. KG
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