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Nc Trek Neo™

FDA UDI

Class II (US FDA UDI)

by Abbott Vascular

Identity

Trade Name
NC TREK NEO™ FDA UDI
Generic Name
Coronary angioplasty balloon catheter, basic FDA UDI
Device Name
NC TREK NEO™ Coronary Dilatation Catheter 2.00 mm x 15 mm / Rapid-Exchange FDA UDI
Model / Reference
1400200-15 FDA UDI
Description
NC TREK NEO™ Coronary Dilatation Catheter 2.00 mm x 15 mm / Rapid-Exchange FDA UDI

Identifiers

Catalog Number
1400200-15 FDA UDI
Primary DI / UDI-DI
08717648232312 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Balloon Length — 15.0000 Millimeter FDA UDI
Balloon Diameter — 2.0000 Millimeter FDA UDI

Category: Coronary angioplasty balloon catheter, basic

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

Similar devices

Also classified as Coronary angioplasty balloon catheter, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbott Vascular

Sources (1)

  • FDA UDI d97128f4-cd94-411e-ba5e-7a2e3e8af5c0 37 fields · synced Jun 1, 2026