InfiltraLong 500

InfiltraLong 500 InfiltraLong Forte catheter 18G x 500mm integrated metal spiral with 30 drill

Registry build 21.09.26
1manufacturer
2catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Registered in Zhejiang. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code BSO
Manufacturer City Province Registered as Device types
Zhejiang Runqiang Medical Instruments Co., Ltd. Jiaxing Zhejiang Contract manufacturer 9

Record

Regulatory record for InfiltraLong 500
Listed by Pajunk Gmbh Medizintechnologie, Germany
FDA product code BSO
Device type Catheter, Conduction, Anesthetic
Device class Class 2
Regulation 21 CFR 868.5120
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Private-label distributor, Complaint-file establishment, Manufacturer
510(k) K080675
Record published 2025-01-30
Record revised 2025-12-01 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date, manufacturing date
Storage Storage environment temperature 10 to 30 °C; Storage environment humidity 20 to 65 % RH
Packaging Pack of 10
Sizes Needle gauge 18 G; length 500 mm

Catalogue Numbers

Catalogue numbers for InfiltraLong 500
Catalogue number Size Status
001158-11A Needle Gauge 18.0 G In distribution
001158-10A In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arrow Teleflex Medical LLC 366
Epimed Epimed International, Inc. 56
Avanos Avanos Medical, Inc. 48
E-Cath Tsui Pajunk Gmbh Medizintechnologie 47
Halyard Avanos Medical, Inc. 34
Infiltralong Pajunk Gmbh Medizintechnologie 25
E-Cath acc. Tsui Pajunk Gmbh Medizintechnologie 21
E-Cath Plus acc. Tsui Pajunk Gmbh Medizintechnologie 17
Epinaut Imedicom Co., Ltd. 16
E-Cath® Plus Tsui® Pajunk Gmbh Medizintechnologie 10
E-Cath® II Tsui® Pajunk Gmbh Medizintechnologie 9
Spinaut-E Imedicom Co., Ltd. 9

Showing 12 of 65. All products under Catheter, Conduction, Anesthetic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K172777 2018-05-03
K152952 2016-07-13
K080675 2008-06-20

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