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Arrow Couvercle Universel

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 271119

by Fournitures Hospitalieres Industrie

Identity

Trade Name
ARROW COUVERCLE UNIVERSEL EUDAMED
ARROW Short Stem Humeral System FDA UDI
Generic Name
Instrument tray cover, reusable FDA UDI
Device Name
TRAYS, LIDS, MATS EUDAMED
Model / Reference
271119 EUDAMED
271119- ARROW COUVERCLE UNIVERSEL FDA UDI

Identifiers

Primary DI / UDI-DI
03661489711190 EUDAMEDFDA UDI
Basic UDI-DI
3661489PANIERCIAH EUDAMED
Direct Marketing DI
03661489711190 EUDAMED
510(k) Number
K202024 FDA UDI
FDA Product Code
PHX FDA UDI
HSD FDA UDI
KWS FDA UDI
EMDN Code
V0499 CLINICAL USE CONTAINERS (NON-IVD) - OTHER EUDAMED
GMDN Term
Instrument tray cover, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
888.3660 FDA UDI
888.3690 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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

No

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: Instrument transport trolley system

Arrow Couvercle Universel by Fournitures Hospitalieres Industrie — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument transport trolley system.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
FR-MF-000000819

Sources (2)

  • EUDAMED 1e412ae7-fd8f-43cf-8729-b47b99f6d68d 61 fields · synced Jul 9, 2026
  • FDA UDI b22b7acd-8298-42be-961d-3fe3c3087901 33 fields · synced May 30, 2026