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Swaromed 1083

by TYROLMED GmbH 2 variants

Swaromed 1083 (6000068N) is a Class II device made by TYROLMED GmbH, listed in FDA GUDID since 10 Oct 2017 (UDI-DI 19120026222656), 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 Number19120026222656 UDI-DI Date10 Oct 2017ListedStatusListed 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  • Withdrawn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
Swaromed
Generic name
Electrocardiographic electrode, single-use
Model / Ref / Catalog
1083, 6000068N
Primary DI / UDI-DI
19120026222656
FDA product code
DRX
GMDN term
Electrocardiographic electrode, single-use
Device class
Class II
Regulation number
870.2360
GUDID distribution status
In Commercial Distribution

Related devices

Category: Electrocardiographic electrode, single-use

Similar devices in this category

Other devices filed under Electrocardiographic electrode, single-use.

Other devices from TYROLMED GmbH

See all devices from TYROLMED GmbH →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)