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Sensimatic™

FDA UDI

Class II (US FDA UDI)

by Parkell, Inc.

Identity

Trade Name
Sensimatic™ FDA UDI
Generic Name
Electrosurgical handpiece, reusable FDA UDI
Device Name
Electrode Handpiece and Cable for Sensimatic® 700SE FDA UDI
Model / Reference
D702 FDA UDI
Description
Electrode Handpiece and Cable for Sensimatic® 700SE FDA UDI

Identifiers

Catalog Number
D702 FDA UDI
Primary DI / UDI-DI
00810000520763 FDA UDI
FDA Product Code
EKZ FDA UDI
GMDN Term
Electrosurgical handpiece, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4920 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Electrosurgical handpiece, reusable

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

Similar devices

Also classified as Electrosurgical handpiece, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Parkell, Inc.

Sources (1)

  • FDA UDI 721b389c-b7dd-4c9a-8401-ede807180074 35 fields · synced Jun 8, 2026