Nautica

Micro Catheter

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number
17510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (3), Shanghai (1), Guangdong (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code KRA
Manufacturer City Province Registered as Device types
Shanghai Wallaby Medical Technologies Co., Inc. Shanghai Shanghai Contract manufacturer 5
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Suzhou Zenith Vascular Scitech Limited Suzhou Jiangsu Manufacturer 6
Suzhou Hengrui Hongyuan Medical Co., Ltd. Suzhou Jiangsu Manufacturer 3
Vascupatent Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Manufacturer 1

Record

Regulatory record for Nautica
Listed by Micro Therapeutics, Inc., United States
FDA product code KRA
Device type Catheter, Continuous Flush
Device class Class 2
Regulation 21 CFR 870.1210
510(k) K093750
Record published 2015-10-09
Record revised 2024-05-16 (version 11)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Special storage condition: Keep dry;Avoid extreme temperatures; Storage environment temperature 50 to 90 °F
Sizes Length 150 cm

Catalogue Numbers

Catalogue numbers for Nautica
Catalogue number Size Status
105-5094-153 Length 150 cm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Fountain® Merit Medical Systems, Inc. 154
PulseSpray AngioDynamics, Inc. 149
Merit Maestro® Merit Medical Systems, Inc. 143
Phenom™ Catheter Cathera, Inc. 103
UniFuse AngioDynamics, Inc. 84
CXI Cook Incorporated 48
Uni-Fuse+ AngioDynamics, Inc. 32
Prowler Medos International Sàrl 27
Truwave, Vamp Edwards Lifesciences Technology Sarl 26
ICU Medical ICU Medical, Inc 21
Cantata Cook Incorporated 20
Truwave, Vamp Plus Edwards Lifesciences Technology Sarl 19

Showing 12 of 149. All products under Catheter, Continuous Flush

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K113289 2012-08-01
K090870 2009-05-01
K051990 2006-01-04
K042187 2004-09-02
K034036 2004-02-13
K031992 2003-08-07
K030688 2003-03-28
K024122 2003-03-07
K024118 2003-02-03
K010004 2001-02-13
K002723 2000-09-28
K001966 2000-07-20
K993672 2000-01-04
K974473 1998-06-17
K980104 1998-04-10
K964868 1997-05-20
K954020 1996-01-02

Recalls Naming This Product

2 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Nautica
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Covidien 510(k) number 2022-06-30 Class II Under Investigation by firm Outer carton packaging of microcatheters were exposed to wet substance during transport. 8 units
Covidien 510(k) number 2022-06-30 Class II Under Investigation by firm Outer carton packaging of microcatheters were exposed to wet substance during transport. 2 units

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer