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Endowrist 03

by Intuitive Surgical, Inc. 3 variants

Endowrist 03 (48645B) is a Class II device made by Intuitive Surgical, Inc., listed in FDA GUDID since 22 Sep 2015 (UDI-DI 00886874103890), 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 Number00886874103890 UDI-DI Date22 Sep 2015ListedStatusListed 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  • Withdrawn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
Endowrist
Generic name
Surgical staple loading unit, non-cutting
Model / Ref / Catalog
03, 48645B
Primary DI / UDI-DI
00886874103890
FDA product code
GDW
GMDN term
Surgical staple loading unit, non-cutting
Device class
Class II
Regulation number
878.4750
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional
Size
Depth — 3.5 Millimeter

Related devices

Category: Surgical staple loading unit, non-cutting

Similar devices in this category

Other devices filed under Surgical staple loading unit, non-cutting.

Other devices from Intuitive Surgical, Inc.

See all devices from Intuitive Surgical, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)