Museux Tenaculum Forceps, 24cm (Curved Sideway) 8 mm (UDI +G072RAE42008R0T)
Manufactured by Rhein Enterprises (Pvt) Ltd
Device Regulatory Overview
The Museux Tenaculum Forceps, 24cm (Curved Sideway) 8 mm (Model/Catalog Number: RAE-420-08R) is a medical device manufactured by Rhein Enterprises (Pvt) Ltd. This product is indexed under FDA Product Code / Category Classification L03130401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RAE-420-08R
- Product Code / EMDN
- L03130401
- Device Name
- Reusable, Stainless Steel, Non-Sterile Surgical Forceps
- Database Sync Date
- 2026-08-09 16:29:06
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 Museux Tenaculum Forceps, 24cm (Curved Sideway) 8 mm?
The registered manufacturer of record for Museux Tenaculum Forceps, 24cm (Curved Sideway) 8 mm is Rhein Enterprises (Pvt) Ltd.
What is the Primary UDI-DI identifier for Museux Tenaculum Forceps, 24cm (Curved Sideway) 8 mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +G072RAE42008R0T.
What classification code is assigned to this device?
This device is registered under product classification code L03130401.
Similar Classification Devices (L03130401)
Other Devices by Rhein Enterprises (Pvt) Ltd
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