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SeQure

FDA UDI

Class II (US FDA UDI)

by Accurate Medical Therapeutics, Ltd.

Identity

Trade Name
SeQure FDA UDI
Generic Name
Vascular microcatheter FDA UDI
Device Name
SeQure Microcatheter - 2.7 Fr., 130 cm, used with Medium Beads FDA UDI
Model / Reference
SQ27_MB_130 FDA UDI
Description
SeQure Microcatheter - 2.7 Fr., 130 cm, used with Medium Beads FDA UDI

Identifiers

Primary DI / UDI-DI
07290017268040 FDA UDI
510(k) Number
K173430 FDA UDI
FDA Product Code
DQO FDA UDI
GMDN Term
Vascular microcatheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vascular microcatheter

SeQure by Accurate Medical Therapeutics, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular microcatheter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bb3b97f0-6336-421e-8f22-e636a103979c 35 fields · synced May 30, 2026