Non-Sterile Single Use Jansen Dissecting Forceps Bayonet Shaped 160mm (UDI +G075BTBD88000K)
Manufactured by Beauty Teck International (Pvt) Ltd
Device Regulatory Overview
The Non-Sterile Single Use Jansen Dissecting Forceps Bayonet Shaped 160mm (Model/Catalog Number: BTBD8800) is a medical device manufactured by Beauty Teck International (Pvt) Ltd. This product is indexed under FDA Product Code / Category Classification K01020104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BTBD8800
- Product Code / EMDN
- K01020104
- Device Name
- Non-Sterile Single Use Jansen Dissecting Forceps Bayonet Shaped 160mm
- Database Sync Date
- 2026-08-09 16:28:47
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Non-Sterile Single Use Jansen Dissecting Forceps Bayonet Shaped 160mm?
The registered manufacturer of record for Non-Sterile Single Use Jansen Dissecting Forceps Bayonet Shaped 160mm is Beauty Teck International (Pvt) Ltd.
What is the Primary UDI-DI identifier for Non-Sterile Single Use Jansen Dissecting Forceps Bayonet Shaped 160mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G075BTBD88000K.
What classification code is assigned to this device?
This device is registered under product classification code K01020104.
Similar Classification Devices (K01020104)
Other Devices by Beauty Teck International (Pvt) Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint