Cragg-McNamara

Valved Infusion Catheter

Registry build 21.09.26
12manufacturers in China registered for this device type
29catalogue numbers in this listing
4510(k) clearances naming this product code

Who Else Makes It

Concentrated in Shandong (3), Guangdong (3), Jiangsu (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FOZ
Manufacturer City Province Registered as Device types
Amsino Medical (Shanghai) Co., Ltd. Shanghai Shanghai Contract manufacturer 22
Bioxin Medical Co., Ltd. Weihai Shandong Contract manufacturer 8
Weihai Jierui Medical Products Co., Ltd. Weihai Shandong Contract manufacturer 3
Becton Dickinson Medical Devices Co., Ltd. Suzhou Suzhou Jiangsu Contract manufacturer 2
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Zhejiang Kindly Medical Devices Co., Ltd. Wenzhou Zhejiang Contract manufacturer 16
Terumo Medical Products (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 7
Shandong Ande Healthcare Apparatus Co., Ltd. Zibo Shandong Manufacturer 7
Jiangxi Sanxin Medtec Co., Ltd. Nanchang Jiangxi Manufacturer 6
Haolang Technology (Foshan) Limited Corporation Foshan Guangdong Contract manufacturer 6
Guangdong Baihe Medical Technology Co., Ltd. Foshan Guangdong Contract manufacturer 4
Foshan Special Medical Co., Ltd. Foshan Guangdong Manufacturer 3

Record

Regulatory record for Cragg-McNamara
Listed by Micro Therapeutics, Inc., United States
FDA product code FOZ
Device type Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Device class Class 2
Regulation 21 CFR 880.5200
510(k) K940634
Record published 2015-10-09
Record revised 2022-08-19 (version 8)

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 Storage environment temperature 50 to 90 °F; Special storage condition: Keep dry;Avoid extreme temperatures;AVOID DIRECT SUNLIGHT
Sizes Length 40 to 135 cm; catheter gauge 4 to 5 Fr

Catalogue Numbers

Catalogue numbers for Cragg-McNamara
Catalogue number Size Status
41043-01 Length 40 cm In distribution
41058-01 Length 135 cm In distribution
41049-01 Length 100 cm In distribution
41055-01 Length 135 cm In distribution
41060-01 Length 135 cm In distribution
41046-01 Length 65 cm In distribution
41042-01 Length 135 cm In distribution
41033-01 Length 40 cm In distribution
41052-01 Length 100 cm In distribution
41050-01 Length 100 cm In distribution
41041-01 Length 135 cm In distribution
41051-01 Length 100 cm In distribution
41054-01 Length 100 cm In distribution
41036-01 Length 65 cm In distribution
41039-01 Length 100 cm In distribution
41032-01 Length 40 cm In distribution
41048-01 Length 65 cm In distribution
41059-01 Length 135 cm In distribution
41037-01 Length 100 cm In distribution
41035-01 Length 65 cm In distribution
41040-01 Length 135 cm In distribution
41038-01 Length 100 cm In distribution
41047-01 Length 65 cm In distribution
41034-01 Length 65 cm In distribution
41053-01 Length 100 cm In distribution
41057-01 Length 135 cm In distribution
41056-01 Length 135 cm In distribution
41045-01 Length 40 cm In distribution
41044-01 Length 40 cm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arrow Teleflex Medical LLC 2,368
Cook Cook Incorporated 250
Cook Spectrum Cook Incorporated 225
Jelco ICU Medical, Inc 104
Medline Medline Industries, Inc. 95
Deltaven Fast Flash Delta Med SpA 77
Deltaven Delta Med SpA 73
PowerGlide Pro Bard Access Systems, Inc. 63
Peripheral Catheter Insertion Kit Bard Access Systems, Inc. 62
Able Central Venous Catheter Guangdong Baihe Medical Technology Co., Ltd. 62
Curaplex Bound Tree Medical, LLC 61
BD Cathena™ Safety IV Catheter Becton, Dickinson AND Company 59

Showing 12 of 285. All products under Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K021139 2002-04-17
K011937 2001-08-28
K953335 1996-01-23
K940634 1994-10-14

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