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Pipeline TM Flex Embolization Device with Shield Technology TM
FDA UDIClass III (US FDA UDI)
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
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
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Also classified as Bare-metal intracranial vascular stent.
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Cleared under the same submission
P100018 also covers:
- PIPELINE — Micro Therapeutics, Inc.
- PIPELINE — Micro Therapeutics, Inc.
- PIPELINE — Micro Therapeutics, Inc.
- PIPELINE — Micro Therapeutics, Inc.
- PIPELINE — Micro Therapeutics, Inc.
- PIPELINE — Micro Therapeutics, Inc.
- PIPELINE — Micro Therapeutics, Inc.
- PIPELINE — Micro Therapeutics, Inc.
- PIPELINE — Micro Therapeutics, Inc.
- PIPELINE — Micro Therapeutics, Inc.
- PIPELINE — Micro Therapeutics, Inc.
- PIPELINE — Micro Therapeutics, Inc.
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 III | Pending data |
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Manufacturer
- Manufacturer
- Micro Therapeutics, Inc.
Sources (1)
- FDA UDI 52815261-6ae3-4037-b1b3-800b137e20c3 35 fields · synced May 30, 2026