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da Vinci Energy

FDA UDI

Class II (US FDA UDI)

by Intuitive Surgical, Inc.

Identity

Trade Name
da Vinci Energy FDA UDI
Generic Name
Electrical-only medical device connection adaptor, reusable FDA UDI
Device Name
Da Vinci Monopolar and Bipolar Adapters FDA UDI
Model / Reference
378896 FDA UDI
Description
Da Vinci Monopolar and Bipolar Adapters FDA UDI

Identifiers

Primary DI / UDI-DI
00886874124000 FDA UDI
510(k) Number
K241621 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrical-only medical device connection adaptor, reusable 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: Electrical-only medical device connection adaptor, reusable

da Vinci Energy by Intuitive Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection adaptor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Intuitive Surgical, Inc.

Sources (1)

  • FDA UDI 92ac915b-d575-48eb-a9f3-fb88ff03427d 34 fields · synced Jun 9, 2026