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EndoWrist

FDA UDI

Class II (US FDA UDI)

by Intuitive Surgical, Inc.

Identity

Trade Name
EndoWrist FDA UDI
Generic Name
Surgical mist irrigation tip FDA UDI
Device Name
CLEARFIELD TUBING FOR STABILIZER FDA UDI
Model / Reference
420185 FDA UDI
Description
CLEARFIELD TUBING FOR STABILIZER FDA UDI

Identifiers

Primary DI / UDI-DI
00886874111550 FDA UDI
FDA Product Code
NAY FDA UDI
GMDN Term
Surgical mist irrigation tip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical mist irrigation tip

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

Similar devices

Also classified as Surgical mist irrigation tip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c9f42df3-5b52-4a80-b6c8-43cff023187a 33 fields · synced Jun 9, 2026