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Single Use Cannula V

FDA UDI

Class II (US FDA UDI)

by Olympus Medical Systems Corporation

Identity

Trade Name
Single Use Cannula V FDA UDI
Generic Name
ERCP catheter, non-balloon, non-electrical, single-use FDA UDI
Model / Reference
PR-V434Q FDA UDI

Identifiers

Primary DI / UDI-DI
04953170183812 FDA UDI
FDA Product Code
ODD FDA UDI
GMDN Term
ERCP catheter, non-balloon, non-electrical, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: ERCP catheter, non-balloon, non-electrical, single-use

Single Use Cannula V by Olympus Medical Systems Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ERCP catheter, non-balloon, non-electrical, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 11cf7cde-e92f-4b3f-a74c-4d095a2e7b8d 33 fields · synced May 30, 2026