PLASTI-MED (UDI 08698573033499)
Manufactured by Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti.
Device Regulatory Overview
The PLASTI-MED (Model/Catalog Number: 489 261 S) is a medical device manufactured by Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti.. This product is indexed under FDA Product Code / Category Classification R020106 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 489 261 S
- Product Code / EMDN
- R020106
- Device Name
- BREATHING CIRCUITSMOOTHBORE ADULT IPPB,STERILE
- Database Sync Date
- 2026-08-09 17:04:49
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 PLASTI-MED?
The registered manufacturer of record for PLASTI-MED is Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti..
What is the Primary UDI-DI identifier for PLASTI-MED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698573033499.
What classification code is assigned to this device?
This device is registered under product classification code R020106.
Similar Classification Devices (R020106)
Other Devices by Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti.
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