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Pipeline TM Flex Embolization Device with Shield Technology TM

FDA UDI

Class III (US FDA UDI)

by Micro Therapeutics, Inc.

Identity

Trade Name
Pipeline TM Flex Embolization Device with Shield Technology TM FDA UDI
Generic Name
Bare-metal intracranial vascular stent FDA UDI
Device Name
STENT PED2-350-18 V08 MDR FDA UDI
Model / Reference
PED2-350-18 FDA UDI
Description
STENT PED2-350-18 V08 MDR FDA UDI

Identifiers

Primary DI / UDI-DI
00763000449018 FDA UDI
PMA Number
P100018 FDA UDI
FDA Product Code
OUT FDA UDI
GMDN Term
Bare-metal intracranial vascular stent FDA UDI

Classification

Device Class
Class III FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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
MRI Safety
MR Conditional FDA UDI

Category: Bare-metal intracranial vascular stent

Pipeline TM Flex Embolization Device with Shield Technology TM by Micro Therapeutics, Inc. — Class III — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Bare-metal intracranial vascular stent.

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 52815261-6ae3-4037-b1b3-800b137e20c3 35 fields · synced May 30, 2026