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Tsi Cs-0070-P

by Tedan Surgical Innovations, L.L.C.

Tsi Cs-0070-P is a Class I device made by Tedan Surgical Innovations, L.L.C., listed in FDA GUDID since 11 Oct 2018 (UDI-DI 00843059122466), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00843059122466 UDI-DI Date11 Oct 2018ListedStatusListed 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  • Withdrawn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
Tsi
Generic name
Surgical retractor/retraction system blade, reusable
Model / reference
CS-0070-P
Primary DI / UDI-DI
00843059122466
FDA product code
MDM
GMDN term
Surgical retractor/retraction system blade, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical retractor/retraction system blade, reusable

Other devices from TeDan Surgical Innovations, Inc.

See all devices from TeDan Surgical Innovations, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)