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WasherCap™ Inserter 9mm & 10mm

EUDAMEDFDA UDI

Class I (EU MDR)

Ref ATMWCIN 42

by Abanza Tecnomed, S.l.

Identity

Trade Name
WasherCap™ Inserter 9mm & 10mm EUDAMEDFDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name
WasherCap™ Inserter 9mm &10mm EUDAMED
Instrument used to place the cap of the WasherCap™ Fixation System at the entrance of the tunnel. FDA UDI
Model / Reference
ATMWCIN 42 EUDAMED
21 FDA UDI
Description
Instrument used to place the cap of the WasherCap™ Fixation System at the entrance of the tunnel. FDA UDI

Identifiers

Primary DI / UDI-DI
08437019739508 EUDAMEDFDA UDI
Basic UDI-DI
B-08437019739508 EUDAMED
FDA Product Code
LXH FDA UDI
EMDN Code
L091104 ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE EUDAMED
GMDN Term
Orthopaedic inorganic implant inserter/extractor, 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

Category: Orthopaedic implant impactor, reusable

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

Similar devices

Also classified as Orthopaedic implant impactor, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
ES-MF-000007530

Sources (2)

  • EUDAMED c60cb0ac-cf2e-4728-ad25-d73e80fe3fce 61 fields · synced Jun 19, 2026
  • FDA UDI 7bd35a22-e858-45af-88e1-ecb0d46f1e9c 34 fields · synced May 30, 2026