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Emboshield Nav6

FDA UDI

Class II (US FDA UDI)

by Abbott Vascular

Identity

Trade Name
EMBOSHIELD NAV6 FDA UDI
Generic Name
Embolic protection filtering guidewire FDA UDI
Device Name
Emboshield NAV6 Embolic Protection System 5.0 mm x 190 cm FDA UDI
Model / Reference
22437-19 FDA UDI
Description
Emboshield NAV6 Embolic Protection System 5.0 mm x 190 cm FDA UDI

Identifiers

Catalog Number
22437-19 FDA UDI
Primary DI / UDI-DI
08717648137747 FDA UDI
FDA Product Code
NTE 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

Emboshield Nav6 by Abbott Vascular — 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
Abbott Vascular

Sources (1)

  • FDA UDI 259fe67a-a587-4a32-8639-42f2f710cc81 36 fields · synced Jun 8, 2026