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VesTraveler®

FDA UDI

Class II (US FDA UDI)

by Dongguan TT Medical, Inc.

Identity

Trade Name
VesTraveler® FDA UDI
Generic Name
Coronary angioplasty balloon catheter, basic FDA UDI
Model / Reference
SD27518 FDA UDI

Identifiers

Primary DI / UDI-DI
06934184002397 FDA UDI
510(k) Number
K230374 FDA UDI
FDA Product Code
LOX FDA UDI
GMDN Term
Coronary angioplasty balloon catheter, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5100 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: Coronary angioplasty balloon catheter, basic

VesTraveler® by Dongguan TT Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coronary angioplasty balloon catheter, basic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3b57bec7-3731-4001-87c3-9ac259d36371 33 fields · synced Jun 6, 2026