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JETi

FDA UDI

Class II (US FDA UDI)

by Walk Vascular L.l.c.

Identity

Trade Name
JETi FDA UDI
Generic Name
Suction/irrigation tubing, single-use FDA UDI
Device Name
All In One Suction Tubing FDA UDI
Model / Reference
WVHAND FDA UDI
Description
All In One Suction Tubing FDA UDI

Identifiers

Primary DI / UDI-DI
B139WVHAND0 FDA UDI
FDA Product Code
QEZ FDA UDI
GMDN Term
Suction/irrigation tubing, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5150 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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Suction/irrigation tubing, single-use

JETi by Walk Vascular L.l.c. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suction/irrigation tubing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 86055880-4f74-4df8-ad9e-23cea33b30a0 33 fields · synced May 30, 2026