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Sterylab S.r.l.

Active in EUDAMED

Italyfrom SRN EUDAMED FDA SRN IT-MF-000015830 FEI 3007748770

Devices
534
Registrations
EUDAMEDFDA
FDA recalls
0

What Sterylab S.r.l. makes

STERYLAB S.R.L. makes bone biopsy devices such as MIELO-CAN, BEST-LISAS, and BEN, as well as soft tissue biopsy devices including FAST-CUT, COLT, SPRING-CUT, and BIO-CUT. The company also produces the DRJ2006 device.

The manufacturer's portfolio includes Class II and Class III devices, which are listed in the EUDAMED registry and the FDA 510(k) database. STERYLAB S.R.L. is based in Italy.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue534

Newest first, rows 501-534 of 534

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  • Ata-Cut Ref ATC2211

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGF1412C

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGS1809

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Auto-Core Ref ACR2009T

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGS1611+

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGF1615+

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGS2007+

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Twin-Needle Ref TWN2015MR

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Twin-Needle Ref TWN1715

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Twin-Needle Ref TWN1709

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Histo-Tac Ref HTS2111

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Histo-Cut Ref HCS2011+

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Twin-Needle Ref TWN1720

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Histo-Tac Ref HTS1909

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Full-Opty Ref FLP1706T

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Full-Opty Ref FLP1725

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGF1820+

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGS1620

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Histo-Cut Ref HCI1715

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Full-Opty Ref FLP1825

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Auto-Core Ref ACR2109T

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Full-Opty Ref FLP1611T

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGF1812C

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGF1815MR

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGS2015MR

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Twin-Needle Ref TWN2020MR

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Histo-Tac Ref HTI1609

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Twin-Needle Ref TWN2209MR

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGS2011+

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Histo-Tac Ref HTI1615

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGF2016C

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Ago-Guida Ref AGS1611MR

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • Active Regimes: 510(k) Registry: 510(k) Class:II
  • DRJ2006

    Active Regimes: CE MDR Registry: EUDAMED Class:III

Rows 501-534 of 534

Showing 501-534 of 534

Company details

EUDAMED SRN
IT-MF-000015830
FDA FEI number
3007748770
EU VAT number
10124260158
EUDAMED status
Active
EUDAMED registered name
STERYLAB S.R.L.
Registered address
77/6, Via Magenta, 20017, Rho, Italy
Phone
+39 0293508427
PRRC contact
Flavio Zambelli(public in EUDAMED)

EUDAMED certificates4

4 certificates3 valid, 0 expired, 1 withdrawn or suspendedMDR 4next expiry 7 Sep 2027

EUDAMED certificates (4)

ITALCERT SRL 0426 4 certificates

  • 030-00-00-MDR Active

    Quality assurance EU MDR

    Issued
    29 Aug 2023
    Expires
    28 Aug 2028
  • 012-00-01-MDR Active Supplemented

    Technical documentation EU MDR

    Issued
    27 Mar 2026
    Expires
    6 Feb 2028
    Reason
    Other
  • 003-00-11-MDR Expiring Supplemented Expires in 309 days

    Quality management system EU MDR

    Issued
    29 Sep 2025
    Expires
    7 Sep 2027
    Reason
    Add device or group
  • 011-00-00-MDR Withdrawn

    Quality management system EU MDR

    Issued
    7 Feb 2023
    Expires
    6 Feb 2028
    Reason
    Other