Identity
- Trade Name
- Trevo XP ProVue Retriever FDA UDI
- Generic Name
- Angiographic catheter, single-use FDA UDI
- Device Name
- Procedure Pack FDA UDI
- Model / Reference
- 93067 FDA UDI
- Description
- Procedure Pack FDA UDI
Identifiers
- Catalog Number
- 93067 FDA UDI
- Primary DI / UDI-DI
- 00815742000672 FDA UDI
- GMDN Term
- Angiographic catheter, single-use FDA UDI
Classification
- 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
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Angiographic catheter, single-useThrombectomy suction catheter
Trevo XP ProVue Retriever by Stryker Corp. — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Stryker Corp.
Sources (1)
- FDA UDI bc6ad850-cdb9-482f-a816-92f58325701e 36 fields · synced May 29, 2026