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1.7 mm RenalCryo™ Cryoprobe

by Varian Medical Systems, Inc. 2 variants

Ref DP35-0942-208

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number089947500200133PP Basic UDI-DI 00810563020793UDI-DIDate17 Mar 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number00810563020793 UDI-DI Date18 Feb 2022ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic Name
Ophthalmic surgical procedure kit, non-medicated, single-use
Device Name
Slimline Cryoprobes
Model / Ref / Catalog
DP35-0942-208, RS-17
Primary DI / UDI-DI
00810563020793
Basic UDI-DI
089947500200133PP
510(k) Number
FDA Product Code
GEH
EMDN Code
Z120102 Cryosurgery equipment
GMDN Term
Ophthalmic surgical procedure kit, non-medicated, single-use
Device Class
Class IIb EUDAMED
Class II GUDID
Regulation Number
878.4350
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class IIb
GUDID
Class II

Manufacturer details

EUDAMED SRN
US-MF-000007453
Authorised representative
Siemens Healthineers Nederland B.V. NL-AR-000000803

Other devices from Varian Medical Systems, Inc

See all devices from Varian Medical Systems, Inc →

Properties

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

Other properties (19)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No