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5302025032

by Stryker Corp.

Ref 5302-025-032Model 08858251002052S5

5302025032 (5302-025-032) is a device classified as Class IIa in the EU and Class I in the US made by Stryker Corp., registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI 08858251002052S5) and listed in FDA GUDID since 23 Sep 2018 (UDI-DI 07613153005155), active as of 7 Nov 2026.

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

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251002052S5 Basic UDI-DI 07613153005155UDI-DIDate2 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07613153005155 UDI-DI Date23 Sep 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251002052S5 registered 2 Nov 2026 Active
  • FDA GUDID UDI-DI 07613153005155 listed 23 Sep 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 07613153005155
  2. Registered EUDAMED 08858251002052S5

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  • Withdrawn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
Surgical saw blade, sagittal, single-use
Device name
CCA Micro Blades
Model / Ref / Catalog
08858251002052S5, 5302-025-032, 5302025032
Primary DI / UDI-DI
07613153005155
Basic UDI-DI
08858251002052S5
FDA product code
GFA
EMDN code
V010302 Blades without safety systems, single-use - not included in other classes
GMDN term
Surgical saw blade, sagittal, single-use
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
878.4820
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Size
Depth — 26.0 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / referenceEUDAMED
08858251002052S5
5302-025-032
GUDID
5302025032
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Surgical saw blade, sagittal, single-use

Similar devices in this category

Other devices filed under BLADES WITHOUT SAFETY SYSTEMS, SINGLE-USE - NOT INCLUDED IN OTHER CLASSES.

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)