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SectionStar 810-00001

by Clarapath, Inc.

SectionStar 810-00001 is a Class I device made by Clarapath, Inc., listed in FDA GUDID since 16 Aug 2024 (UDI-DI 00198168976302), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00198168976302 UDI-DI Date16 Aug 2024ListedStatusListed GUDID: not 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  • Withdrawn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
SectionStar
Generic name
Rotary microtome IVD
Model / reference
810-00001
Primary DI / UDI-DI
00198168976302
FDA product code
IDO
GMDN term
Rotary microtome IVD
Device class
Class I
Regulation number
864.3010
GUDID distribution status
Not in Commercial Distribution

Similar devices

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

Other devices from Clarapath, Inc.

See all devices from Clarapath, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)