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SportMeds Instruments

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 05.13.10.0138Model Sportsmed Hand Instrument

by Medacta International

Identity

Trade Name
Suture Cutter Open WL165 Forceps Handle EUDAMED
SportMeds Instruments FDA UDI
Generic Name
Arthroscopic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Suture Cutter Open WL165 Forceps Handle Removable locking handle FDA UDI
Model / Reference
05.13.10.0138 EUDAMEDFDA UDI
Sportsmed Hand Instrument EUDAMED
Description
Suture Cutter Open WL165 Forceps Handle Removable locking handle FDA UDI

Identifiers

Primary DI / UDI-DI
07630971256279 EUDAMEDFDA UDI
Basic UDI-DI
764014274LSR0141N00BP EUDAMED
Direct Marketing DI
07630971256279 EUDAMED
FDA Product Code
NBH FDA UDI
EMDN Code
L1913 ARTHROSCOPIC SURGERY HANDPIECES, REUSABLE EUDAMED
GMDN Term
Arthroscopic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.1100 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Arthroscopic surgical procedure kit, non-medicated, reusable

SportMeds Instruments by Medacta International — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 09866a51-513d-4a89-9457-eca95a515f22 33 fields · synced Oct 8, 2026
  • EUDAMED 0ffadda7-3d17-4d0b-b29a-77c2570424e3 61 fields · synced Oct 8, 2026