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SchurSign 1.5-5

by Surgmark GmbH

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04262491960003 UDI-DI Date29 Nov 2024ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
SchurSign
Generic Name
Radiological image marker, implantable
Model / Reference
SchurSign 1.5-5
Primary DI / UDI-DI
04262491960003
510(k) Number
FDA Product Code
NEU
GMDN Term
Radiological image marker, implantable
Device Class
Class II
Regulation Number
878.4300
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Related devices

Category: Radiological image marker, implantable

Other devices from Surgmark GmbH

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No