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Pv Glidesafe Hp

FDA UDI

Class II (US FDA UDI)

by Cynosure, LLC

Identity

Trade Name
PV GLIDESAFE HP FDA UDI
Generic Name
Electrosurgical system FDA UDI
Device Name
PV GLIDESAFE HP & CABLE 20MM INTL (3 HP) FDA UDI
Model / Reference
P220HPD FDA UDI
Description
PV GLIDESAFE HP & CABLE 20MM INTL (3 HP) FDA UDI

Identifiers

Catalog Number
P220HPD FDA UDI
Primary DI / UDI-DI
00841494105327 FDA UDI
510(k) Number
K102698 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical system 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical system

Pv Glidesafe Hp by Cynosure, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cynosure, LLC

Sources (1)

  • FDA UDI cf73cf4e-4aa5-4865-9b71-0941b0c39086 35 fields · synced May 30, 2026