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Venom Multigen 2

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
VENOM MULTIGEN 2 FDA UDI
Generic Name
Percutaneous radio-frequency ablation probe cannula, reusable FDA UDI
Device Name
150MM ELECTRODE FDA UDI
Model / Reference
8400-825-015 FDA UDI
Description
150MM ELECTRODE FDA UDI

Identifiers

Catalog Number
8400-825-015 FDA UDI
Primary DI / UDI-DI
07613327173697 FDA UDI
FDA Product Code
GXD FDA UDI
GMDN Term
Percutaneous radio-frequency ablation probe cannula, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4400 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 150.0 Millimeter FDA UDI

Category: Percutaneous radio-frequency ablation probe cannula, reusable

Venom Multigen 2 by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Percutaneous radio-frequency ablation probe cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI bba5aabf-7623-4f06-bfd4-c70127815c26 37 fields · synced Jun 6, 2026