Forceps, Biopsy, Rigid Endoscopic (UDI 04049203183987)
Manufactured by STEMA Medizintechnik GmbH
Device Regulatory Overview
The Forceps, Biopsy, Rigid Endoscopic (Model/Catalog Number: AC-101-212-OT) is a medical device manufactured by STEMA Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification L060403 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AC-101-212-OT
- Product Code / EMDN
- L060403
- Device Name
- Forceps, Biopsy, Rigid Endoscopic
- Database Sync Date
- 2026-08-09 16:29:59
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 Forceps, Biopsy, Rigid Endoscopic?
The registered manufacturer of record for Forceps, Biopsy, Rigid Endoscopic is STEMA Medizintechnik GmbH.
What is the Primary UDI-DI identifier for Forceps, Biopsy, Rigid Endoscopic?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04049203183987.
What classification code is assigned to this device?
This device is registered under product classification code L060403.
Similar Classification Devices (L060403)
Other Devices by STEMA Medizintechnik GmbH
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