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Clarapath™ SectionStar™ 810-00002

by Clarapath, Inc.

Clarapath™ SectionStar™ 810-00002 is a Class I device made by Clarapath, Inc., listed in FDA GUDID since 4 Feb 2025 (UDI-DI 00860012688968), 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 Number00860012688968 UDI-DI Date4 Feb 2025ListedStatusListed 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  • Withdrawn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
Clarapath™ SectionStar™
Generic name
Rotary microtome IVD
Model / reference
810-00002
Primary DI / UDI-DI
00860012688968
FDA product code
IDO
GMDN term
Rotary microtome IVD
Device class
Class I
Regulation number
864.3010
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rotary microtome IVD

Similar devices

Other devices filed under FDA product code IDO (Microtome, Rotary).

Other devices from Clarapath, Inc.

See all devices from Clarapath, Inc. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)