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Single-Site 428060

by Intuitive Surgical, Inc.

Single-Site 428060 is a Class II device made by Intuitive Surgical, Inc., listed in FDA GUDID since 8 Jul 2016 (UDI-DI 00886874111970), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00886874111970 UDI-DI Date8 Jul 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Single-Site
Generic name
Laparoscopic access cannula, reusable
Model / reference
428060
Primary DI / UDI-DI
00886874111970
FDA product code
GCJ, NAY
GMDN term
Laparoscopic access cannula, reusable
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Lumen/Inner Diameter — 5 Millimeter

Related devices

Category: Laparoscopic access cannula, reusable

Similar devices in this category

Other devices filed under Laparoscopic access cannula, reusable.

Other devices from Intuitive Surgical, Inc.

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)