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De Soutter Medical S22-059

by De Soutter Medical, Ltd.

De Soutter Medical S22-059 is a Class I device made by De Soutter Medical, Ltd., listed in FDA GUDID since 24 Nov 2022 (UDI-DI 05051471023567), 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 Number05051471023567 UDI-DI Date24 Nov 2022ListedStatusListed 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  • Withdrawn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
De Soutter Medical
Generic name
Surgical saw blade, reciprocating, single-use
Model / Ref / Catalog
S22-059
Primary DI / UDI-DI
05051471023567
FDA product code
GEY
GMDN term
Surgical saw blade, reciprocating, single-use
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical saw blade, reciprocating, single-use

Similar devices in this category

Other devices filed under Surgical saw blade, reciprocating, single-use.

Other devices from De Soutter Medical, Ltd.

See all devices from De Soutter Medical, Ltd. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)