NA (UDI 8982017)
Manufactured by Richard Wolf GmbH
Device Regulatory Overview
The NA (Model/Catalog Number: 8982017) is a medical device manufactured by Richard Wolf GmbH. This product is indexed under FDA Product Code / Category Classification MOK within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
PiezoWave 2 Control Unit, Product Number 100506US, compact myofascial acoustic compression therapy device that enables treatment with piezoe...
RICHARD WOLF TUBE SET FOR TEM, REF 4170.801. Used for the transanal endoscopic microsurgery....
Artholine Punch B 4, 6MM H 1, 6MM, used for the removal of soft tissue, cartilage tissue or other non-osseous tissue via natural or surgica...
Technical Specifications
- Model Number
- 8982017
- Product Code / EMDN
- MOK
- Device Name
- OBTURATOR FOR VAGINOSCOPE OD 4.8MM for WL 113mm, compatible with vaginal scope tube 8982015, reusable
- Database Sync Date
- 2026-08-09 09:26:09
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 NA?
The registered manufacturer of record for NA is Richard Wolf GmbH.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8982017.
What classification code is assigned to this device?
This device is registered under product classification code MOK.
Similar Classification Devices (MOK)
Other Devices by Richard Wolf GmbH
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint