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Sports Med Instruments

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 05.12.10.0005Model Sportsmed Extraction instrument / Removal device / Corkscrew

by Medacta International

Identity

Trade Name
Fork EUDAMED
Sports Med Instruments FDA UDI
Generic Name
Arthroscopic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Ligament Staples Fork FDA UDI
Model / Reference
05.12.10.0005 EUDAMEDFDA UDI
Sportsmed Extraction instrument / Removal device / Corkscrew EUDAMED
Description
Ligament Staples Fork FDA UDI

Identifiers

Primary DI / UDI-DI
07630971283176 EUDAMEDFDA UDI
Basic UDI-DI
764014274LSR0111N00AN EUDAMED
Direct Marketing DI
07630971283176 EUDAMED
FDA Product Code
NBH FDA UDI
EMDN Code
L1999 ARTHROSCOPIC SURGERY INSTRUMENTS, REUSABLE - OTHER 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

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

Sports Med 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 86183baa-da30-4c0d-87c3-e2f21d602756 33 fields · synced Aug 1, 2026
  • EUDAMED 0da94706-a742-4331-a4aa-86a9d2635fe5 61 fields · synced Aug 1, 2026