8F Base Camp system 2.0 90cm

FDA UDI

Class II (US FDA UDI)

by Route 92 Medical, Inc.

Identity

Trade Name: 8F Base Camp system 2.0 90cm FDA UDI
Generic Name: Vascular microcatheter FDA UDI
Device Name: 8F Base Camp system 2.0 90cm FDA UDI
Model / Reference: Gen 2.0 FDA UDI
Description: 8F Base Camp system 2.0 90cm FDA UDI

Identifiers

Catalog Number: REF 5001-2-90B FDA UDI
Primary DI / UDI-DI: 00853799007725 FDA UDI
510(k) Number: K240529 FDA UDI
FDA Product Code: DQY FDA UDI
QJP FDA UDI
GMDN Term: Vascular microcatheter 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Vascular guide-catheter, single-use Vascular microcatheter

8F Base Camp system 2.0 90cm by Route 92 Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Vascular microcatheter.

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Merit Maestro® — Merit Medical Systems, Inc. · Class II
Lantern Delivery Catheter — PENUMBRA, INC. · Class II
Direxion™ Fathom™-16 System — Boston Scientific · Class II

Cleared under the same submission

K240529 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Route 92 Medical, Inc.

Sources (1)

FDA UDI 6cd0995d-4b0a-472c-870a-3b60350755d0 36 fields · synced May 30, 2026