Medivision

FDA UDI

Class II (US FDA UDI)

by Medivision, Inc.

Identity

Trade Name: MEDIVISION FDA UDI
Generic Name: Rigid optical sinoscope FDA UDI
Device Name: ARTHROSCOPE Intended use of MediVision Arthroscope is for orthopedic use in the knee, shoulder, wrist (carpal ligament release), temporal-mandibular joint, ankle, elbow, and plantar fascia release. SINUSCOPE Intended use of MediVision Sinuscope is to allow direct visualization (through the Sinuscope or the video monitor) of the nasal cavity. FDA UDI
Model / Reference: MVA470 FDA UDI
Description: ARTHROSCOPE Intended use of MediVision Arthroscope is for orthopedic use in the knee, shoulder, wrist (carpal ligament release), temporal-mandibular joint, ankle, elbow, and plantar fascia release. SINUSCOPE Intended use of MediVision Sinuscope is to allow direct visualization (through the Sinuscope or the video monitor) of the nasal cavity. FDA UDI

Identifiers

Catalog Number: MVA470 FDA UDI
Primary DI / UDI-DI: 00851328007109 FDA UDI
FDA Product Code: HRX FDA UDI
EOB FDA UDI
GMDN Term: Rigid optical sinoscope FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.1100 FDA UDI
874.4760 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Rigid optical arthroscope, reusable Rigid optical sinoscope

Medivision by Medivision, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical sinoscope.

JEDMED — JEDMED Instrument Company · Class II
BR Surgical, LLC — BR SURGICAL LLC · Class II
SINUSCOPE — Ecleris · Class II
JEDMED — JEDMED Instrument Company · Class II
JEDMED — JEDMED Instrument Company · Class II
AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class II
PrimeSight — SCHÖLLY FIBEROPTIC GmbH · Class II
AED — NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Medivision, Inc.

Sources (1)

FDA UDI 3df64247-518e-4bba-a8f6-f1439e155c1c 34 fields · synced May 30, 2026