PLASTI-MED (UDI 08699412007756)
Manufactured by Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti.
Device Regulatory Overview
The PLASTI-MED (Model/Catalog Number: 160 2003 9 7) 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 A060301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 160 2003 9 7
- Product Code / EMDN
- A060301
- Device Name
- SUCTION BAG FLEXIBLE LINER 2000ML, WITH ANTIFOAM, GEL (WITH TUBE)
- Database Sync Date
- 2026-08-09 16:30:32
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 08699412007756.
What classification code is assigned to this device?
This device is registered under product classification code A060301.
Similar Classification Devices (A060301)
Other Devices by Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti.
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