eudamed_udi
Primary ID: 40505880005612
pulsar® lt 3p (UDI 40505880005612)
Manufactured by h/p/cosmos sports & medical gmbh
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for pulsar® lt 3p - Primary ID 40505880005612
Device Regulatory Overview
The pulsar® lt 3p (Model/Catalog Number: cos30004va02) is a medical device manufactured by h/p/cosmos sports & medical gmbh. This product is indexed under FDA Product Code / Category Classification Z129006 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- cos30004va02
- Product Code / EMDN
- Z129006
- Device Name
- pulsar® lt 3p
- Database Sync Date
- 2026-08-09 16:49:01
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 pulsar® lt 3p?
The registered manufacturer of record for pulsar® lt 3p is h/p/cosmos sports & medical gmbh.
What is the Primary UDI-DI identifier for pulsar® lt 3p?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 40505880005612.
What classification code is assigned to this device?
This device is registered under product classification code Z129006.
Similar Classification Devices (Z129006)
Other Devices by h/p/cosmos sports & medical gmbh
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