ARCHIMED (UDI 08681957013439)
Manufactured by ARŞİMED MEDİKAL KOZM.BİL.İTH.İHR.PAZ. TİC.LTD.ŞTİ.
Device Regulatory Overview
The ARCHIMED (Model/Catalog Number: CB02-G WIGGLE CHILD BED, 2 MOTORS) is a medical device manufactured by ARŞİMED MEDİKAL KOZM.BİL.İTH.İHR.PAZ. TİC.LTD.ŞTİ.. This product is indexed under FDA Product Code / Category Classification V0806010701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CB02-G WIGGLE CHILD BED, 2 MOTORS
- Product Code / EMDN
- V0806010701
- Device Name
- UNIQUE PLUS HOSPITAL BED 5 MOTORS WITH CENTRAL AND DIRECTIONAL LOCK CASTORS
- Database Sync Date
- 2026-08-09 16:29:29
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 ARCHIMED?
The registered manufacturer of record for ARCHIMED is ARŞİMED MEDİKAL KOZM.BİL.İTH.İHR.PAZ. TİC.LTD.ŞTİ..
What is the Primary UDI-DI identifier for ARCHIMED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681957013439.
What classification code is assigned to this device?
This device is registered under product classification code V0806010701.
Similar Classification Devices (V0806010701)
Other Devices by ARŞİMED MEDİKAL KOZM.BİL.İTH.İHR.PAZ. TİC.LTD.ŞTİ.
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