ABDOMINAL TROCAR, REUSABLE (UDI L031202)
Device Regulatory Overview
The ABDOMINAL TROCAR, REUSABLE (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification L031202 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- L031202
- Device Name
- ABDOMINAL TROCAR, REUSABLE
- Database Sync Date
- 2026-08-09 16:18:37
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 ABDOMINAL TROCAR, REUSABLE?
The registered manufacturer of record for ABDOMINAL TROCAR, REUSABLE is .
What is the Primary UDI-DI identifier for ABDOMINAL TROCAR, REUSABLE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is L031202.
What classification code is assigned to this device?
This device is registered under product classification code L031202.
Similar Classification Devices (L031202)
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