gudid
Primary ID: MS2317
MEGASORB (UDI MS2317)
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 MEGASORB - Primary ID MS2317
Device Regulatory Overview
The MEGASORB (Model/Catalog Number: MS2317) is a medical device manufactured by MERIL ENDO SURGERY PRIVATE LIMITED. This product is indexed under FDA Product Code / Category Classification GAM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MS2317
- Product Code / EMDN
- GAM
- Device Name
- Braided coated Polyglycolic Acid Surgical Suture USP
- Database Sync Date
- 2026-08-09 09:29:37
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 MEGASORB?
The registered manufacturer of record for MEGASORB is MERIL ENDO SURGERY PRIVATE LIMITED.
What is the Primary UDI-DI identifier for MEGASORB?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MS2317.
What classification code is assigned to this device?
This device is registered under product classification code GAM.
Similar Classification Devices (GAM)
Other Devices by MERIL ENDO SURGERY PRIVATE LIMITED
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