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MicroMewiTM

FDA UDI

Class II (US FDA UDI)

by Micro Therapeutics, Inc.

Identity

Trade Name
MicroMewiTM FDA UDI
Generic Name
Peripheral vascular intervention infusion catheter FDA UDI
Device Name
INF CATH 41067-01 MICROMEWI V03 FDA UDI
Model / Reference
41067-01 FDA UDI
Description
INF CATH 41067-01 MICROMEWI V03 FDA UDI

Identifiers

Primary DI / UDI-DI
00847536008076 FDA UDI
510(k) Number
K940634 FDA UDI
FDA Product Code
FOZ FDA UDI
GMDN Term
Peripheral vascular intervention infusion catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5200 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Peripheral vascular intervention infusion catheter

MicroMewiTM by Micro Therapeutics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral vascular intervention infusion catheter.

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 da195b2f-5646-4bd8-add3-5d1925f73f5d 36 fields · synced May 30, 2026