← Back to catalogue

Fortress®

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 452384Model FG-08557-001

by Contract Medical International GmbH

Identity

Trade Name
Fortress® EUDAMED
Biotronik Fortress Introducer Sheath System FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
Fortress Introducer Sheath EUDAMED
Introducer Sheath System containing One (1) introducer Sheath with haemostasis valve and One (1) dilator. FDA UDI
Model / Reference
FG-08557-001 EUDAMED
452384 EUDAMED
8F, 65cm, straight FDA UDI
Description
Introducer Sheath System containing One (1) introducer Sheath with haemostasis valve and One (1) dilator. FDA UDI

Identifiers

Catalog Number
452384 FDA UDI
Primary DI / UDI-DI
04251244500955 EUDAMEDFDA UDI
Basic UDI-DI
B-04251244500955 EUDAMED
FDA Product Code
DYB FDA UDI
DRE FDA UDI
EMDN Code
C0599 CARDIOVASCULAR INTRODUCER SHEATHS - OTHER EUDAMED
GMDN Term
Vascular catheter introduction set, nonimplantable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
870.1340 FDA UDI
870.1310 FDA UDI
Market of Registration
Austria EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 65 Centimeter FDA UDI
Lumen/Inner Diameter — 2.88 Millimeter FDA UDI

Fortress® by Contract Medical International GmbH — Class IIa — 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
DE-MF-000007409

Sources (2)

  • EUDAMED c96c8b3e-08e5-4a70-b63e-331dd45d75c9 61 fields · synced May 31, 2026
  • FDA UDI e64739d4-cbdd-4ed1-b6fc-3a1602573288 37 fields · synced May 22, 2026