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Wallach

FDA UDI

Class II (US FDA UDI)

by CooperSurgical, Inc.

Identity

Trade Name
WALLACH FDA UDI
Generic Name
Electrosurgical system FDA UDI
Device Name
Quantum 2000 Electrosurgical Generator (120 VAC) FDA UDI
Model / Reference
909075 FDA UDI
Description
Quantum 2000 Electrosurgical Generator (120 VAC) FDA UDI

Identifiers

Primary DI / UDI-DI
00888937013993 FDA UDI
510(k) Number
K963653 FDA UDI
FDA Product Code
HGI FDA UDI
GMDN Term
Electrosurgical system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4120 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical system

Wallach by CooperSurgical, Inc. — 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

Sources (1)

  • FDA UDI 8d8389c1-4d2a-45a1-ad41-9dfdfd251589 34 fields · synced Jun 9, 2026