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87 NeuGlide Catheter

FDA UDI

Class II (US FDA UDI)

by Piraeus Medical

Identity

Trade Name
87 NeuGlide Catheter FDA UDI
Generic Name
Vascular guide-catheter, single-use FDA UDI
Device Name
The 87 NeuGlide Catheter (103577-002) has an inner diameter of 0.087” (6F compatible), a maximum outer diameter of 0.100”, and a working length of 100 cm. FDA UDI
Model / Reference
103577-002 FDA UDI
Description
The 87 NeuGlide Catheter (103577-002) has an inner diameter of 0.087” (6F compatible), a maximum outer diameter of 0.100”, and a working length of 100 cm. FDA UDI

Identifiers

Catalog Number
103577-002 FDA UDI
Primary DI / UDI-DI
00860010306314 FDA UDI
510(k) Number
K240971 FDA UDI
FDA Product Code
QJP FDA UDI
DQY FDA UDI
GMDN Term
Vascular guide-catheter, single-use 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: Vascular guide-catheter, single-use

87 NeuGlide Catheter by Piraeus Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular guide-catheter, single-use.

Cleared under the same submission

K240971 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Piraeus Medical

Sources (1)

  • FDA UDI 40b219b4-a476-4043-a70c-c6081d160f3b 35 fields · synced May 30, 2026