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JETi™

FDA UDI

Class II (US FDA UDI)

by Abbott Vascular

Identity

Trade Name
JETi™ FDA UDI
Generic Name
Surgical suction system collection container, single-use FDA UDI
Device Name
JETi™ Non-Sterile Canister Set FDA UDI
Model / Reference
WV1500A FDA UDI
Description
JETi™ Non-Sterile Canister Set FDA UDI

Identifiers

Catalog Number
WV1500A FDA UDI
Primary DI / UDI-DI
08717648351389 FDA UDI
FDA Product Code
KDQ FDA UDI
GMDN Term
Surgical suction system collection container, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

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: Surgical suction system collection container, single-use

JETi™ by Abbott Vascular — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical suction system collection container, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott Vascular

Sources (1)

  • FDA UDI b858b9ad-f74b-487f-a672-963629c6bb01 37 fields · synced May 31, 2026