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EndoWrist +1 more model

FDA UDI

Class II (US FDA UDI)

by Intuitive Surgical, Inc.

Identity

Trade Name
EndoWrist;daVinci Si FDA UDI
Generic Name
Self-retaining surgical retractor, reusable FDA UDI
Device Name
STABILIZER FDA UDI
Model / Reference
420182 FDA UDI
Description
STABILIZER FDA UDI

Identifiers

Primary DI / UDI-DI
00886874111529 FDA UDI
FDA Product Code
NAY FDA UDI
GMDN Term
Self-retaining surgical retractor, reusable FDA UDI
Models / Variants
EndoWrist FDA UDI
daVinci Si 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

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

Dimensions & Sizes

Size
Outer Diameter — 12 Millimeter FDA UDI

Category: Self-retaining surgical retractor, reusable

EndoWrist +1 more model by Intuitive Surgical, Inc. — Class II — FDA UDI — listed in FDA GUDID — 2 models — regulatory data on deviCERTS

Similar devices

Also classified as Self-retaining surgical retractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 912e029c-7e16-44c8-8b2b-66e17f434382 34 fields · synced Jun 9, 2026