Dilator, Vascular, Memory 24cm 0.5mm monobloc

FDA UDI

Class II (US FDA UDI)

by Geister Medizin Technik GmbH

Identity

Trade Name: Dilator, Vascular, Memory 24cm 0.5mm monobloc FDA UDI
Generic Name: Vascular dilator, reusable FDA UDI
Device Name: Dilator, Vascular, Memory 24cm 0.5mm monobloc Nitinol FDA UDI
Model / Reference: 21-0090 FDA UDI
Description: Dilator, Vascular, Memory 24cm 0.5mm monobloc Nitinol FDA UDI

Identifiers

Catalog Number: 21-0090 FDA UDI
Primary DI / UDI-DI: 04057034046265 FDA UDI
FDA Product Code: DWP FDA UDI
GMDN Term: Vascular dilator, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.4475 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Vascular dilator, reusable

Dilator, Vascular, Memory 24cm 0.5mm monobloc by Geister Medizin Technik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Geister Medizin Technik GmbH

Sources (1)

FDA UDI c2f39d32-2f3d-423d-a90a-28d7941e6898 35 fields · synced May 31, 2026