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Inserter Coupling Screw 9mm & 10mm

EUDAMEDFDA UDI

Class I (EU MDR)

Ref ATMWCIN62

by Abanza Tecnomed, S.l.

Identity

Trade Name
Inserter Coupling Screw 9mm & 10mm EUDAMEDFDA UDI
Generic Name
Orthopaedic implantation sleeve, reusable FDA UDI
Device Name
Inserter Coupling Screw 9mm &10mm EUDAMED
Instrument used to couple the cap of the WasherCap™ Fixation System to the inserter, threading it into the inserter until the “device-inserter” assembly is fully engaged. FDA UDI
Model / Reference
ATMWCIN62 EUDAMED
21 FDA UDI
Description
Instrument used to couple the cap of the WasherCap™ Fixation System to the inserter, threading it into the inserter until the “device-inserter” assembly is fully engaged. FDA UDI

Identifiers

Primary DI / UDI-DI
08437019739577 EUDAMEDFDA UDI
Basic UDI-DI
B-08437019739577 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L098099 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER ACCESSORIES EUDAMED
GMDN Term
Orthopaedic implantation sleeve, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
Market of Registration
Spain 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

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

Inserter Coupling Screw 9mm & 10mm by Abanza Tecnomed, S.l. — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
ES-MF-000007530

Sources (2)

  • EUDAMED e57afb46-f16a-4556-a9f4-2279b42d92ba 61 fields · synced Jul 16, 2026
  • FDA UDI 8d7cb8ce-03f1-4e7d-8e98-9411fc2d5e2f 34 fields · synced May 30, 2026