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EZ Bent Tip

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
EZ Bent Tip FDA UDI
Generic Name
Embolic protection filtering guidewire FDA UDI
Device Name
Retrieval Sheath FDA UDI
Model / Reference
H749501001500 FDA UDI
Description
Retrieval Sheath FDA UDI

Identifiers

Primary DI / UDI-DI
08714729479109 FDA UDI
FDA Product Code
NFA FDA UDI
GMDN Term
Embolic protection filtering guidewire FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 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: Embolic protection filtering guidewire

EZ Bent Tip by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Embolic protection filtering guidewire.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI a60b0065-eb53-472a-a162-e0fbba749e6e 34 fields · synced May 30, 2026