GPAD BACK BAR 3MM 260 LARGE PAD (UDI 08685077962059)
Manufactured by TEDOB PRODÜKSİYON SAĞLIK VE GIDA SAN. VE TİC. LTD. ŞTİ.
Device Regulatory Overview
The GPAD BACK BAR 3MM 260 LARGE PAD (Model/Catalog Number: BB3260L) is a medical device manufactured by TEDOB PRODÜKSİYON SAĞLIK VE GIDA SAN. VE TİC. LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification Y061219 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BB3260L
- Product Code / EMDN
- Y061219
- Device Name
- GPAD PUCTUS CARINATUM POSTURE CORRECTION BRACE
- Database Sync Date
- 2026-08-09 16:51:02
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 GPAD BACK BAR 3MM 260 LARGE PAD?
The registered manufacturer of record for GPAD BACK BAR 3MM 260 LARGE PAD is TEDOB PRODÜKSİYON SAĞLIK VE GIDA SAN. VE TİC. LTD. ŞTİ..
What is the Primary UDI-DI identifier for GPAD BACK BAR 3MM 260 LARGE PAD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08685077962059.
What classification code is assigned to this device?
This device is registered under product classification code Y061219.
Similar Classification Devices (Y061219)
Other Devices by TEDOB PRODÜKSİYON SAĞLIK VE GIDA SAN. VE TİC. LTD. ŞTİ.
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