eudamed_udi
Primary ID: 08907265208214
POWER-DROOL (UDI 08907265208214)
Manufactured by Romsons Group Private Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for POWER-DROOL - Primary ID 08907265208214
Device Regulatory Overview
The POWER-DROOL (Model/Catalog Number: SH-2082S) is a medical device manufactured by Romsons Group Private Limited. This product is indexed under FDA Product Code / Category Classification R03010304 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SH-2082S
- Product Code / EMDN
- R03010304
- Device Name
- NEBULIZER: Mask / Mouth Piece with Nebulization Chamber and Tubing.
- Database Sync Date
- 2026-08-09 17:03:32
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 POWER-DROOL?
The registered manufacturer of record for POWER-DROOL is Romsons Group Private Limited.
What is the Primary UDI-DI identifier for POWER-DROOL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08907265208214.
What classification code is assigned to this device?
This device is registered under product classification code R03010304.
Similar Classification Devices (R03010304)
Other Devices by Romsons Group Private Limited
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint