gudid
Primary ID: VMLT-200
MirusTM Ligating Clip (UDI VMLT-200)
Manufactured by MERIL ENDO SURGERY PRIVATE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MirusTM Ligating Clip - Primary ID VMLT-200
Device Regulatory Overview
The MirusTM Ligating Clip (Model/Catalog Number: VMLT-200) is a medical device manufactured by MERIL ENDO SURGERY PRIVATE LIMITED. This product is indexed under FDA Product Code / Category Classification FZP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VMLT-200
- Product Code / EMDN
- FZP
- Device Name
- "Mirus Ligating clip are sterile, single use, implantable device made of implant grade titanium (ISO 5832-2 / ASTM F 67) that are intended for general surgical procedures that require vessel or tissue ligation. Mirus Ligating clips are supplied with multiuse non sterile Mirus Ligating Clip applier, allowing the end user to ligate a wide range of vessels and tissue TM structures, using the Mirus Ligating clips."
- Database Sync Date
- 2026-08-09 09:29:39
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 MirusTM Ligating Clip?
The registered manufacturer of record for MirusTM Ligating Clip is MERIL ENDO SURGERY PRIVATE LIMITED.
What is the Primary UDI-DI identifier for MirusTM Ligating Clip?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VMLT-200.
What classification code is assigned to this device?
This device is registered under product classification code FZP.
Similar Classification Devices (FZP)
Other Devices by MERIL ENDO SURGERY PRIVATE LIMITED
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