gudid
Primary ID: RM0112
MOLLI (UDI RM0112)
Manufactured by STRYKER CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MOLLI - Primary ID RM0112
Device Regulatory Overview
The MOLLI (Model/Catalog Number: RM0112) is a medical device manufactured by STRYKER CORPORATION. This product is indexed under FDA Product Code / Category Classification KDC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RM0112
- Product Code / EMDN
- KDC
- Device Name
- MOLLI re.markable (w/ 12cm Introducer) Single Unit
- Database Sync Date
- 2026-08-09 09:37:43
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 MOLLI?
The registered manufacturer of record for MOLLI is STRYKER CORPORATION.
What is the Primary UDI-DI identifier for MOLLI?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RM0112.
What classification code is assigned to this device?
This device is registered under product classification code KDC.
Similar Classification Devices (KDC)
Other Devices by STRYKER CORPORATION
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint