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Virtuosaph Plus Endoscopic Vessel Harvester

FDA UDI

Class II (US FDA UDI)

by Terumo Cardiovascular Systems Corporation

Identity

Trade Name
Virtuosaph Plus Endoscopic Vessel Harvester FDA UDI
Generic Name
Endoscopic electrosurgical electrode, bipolar, single-use FDA UDI
Model / Reference
VSP550 FDA UDI

Identifiers

Primary DI / UDI-DI
00699753022966 FDA UDI
510(k) Number
K160206 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, bipolar, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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: Endoscopic electrosurgical electrode, bipolar, single-use

Virtuosaph Plus Endoscopic Vessel Harvester by Terumo Cardiovascular Systems Corporation — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Endoscopic electrosurgical electrode, bipolar, single-use.

Cleared under the same submission

K160206 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Terumo Cardiovascular Systems Corporation

Sources (1)

  • FDA UDI c15dac26-49a8-4bbd-b64f-96e2466109af 33 fields · synced Jun 9, 2026