Pounce Sheath

The Pounce Sheath introduces diagnostic or therapeutic devices into blood vessels. It is a sterile, single-use introducer with a hub and hemostasis valve for inserting and removing those…

Registry build 21.09.26

The Pounce Sheath introduces diagnostic or therapeutic devices into blood vessels. It is a sterile, single-use introducer with a hub and hemostasis valve for inserting and removing those devices. A dilator compatible with a 0.035-inch guidewire is included for sheath introduction.

A braided nitinol funnel expands at the distal end when released from the sheath. A slider on the handle deploys and retracts this funnel. The radiopaque marker lies at the distal tip while the funnel is covered and proximal to the funnel when it is deployed.

Listed Item

Pounce Sheath 16Fr

Valve and Aspiration

Pressing the base of the hub opens the hemostasis valve for device passage. The aspiration assembly includes tubing, a stopcock and a connection for the supplied 60 cc locking syringe. It also permits delivery of contrast or saline.

13manufacturers in China registered for this device type
2catalogue numbers in this listing
3510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (5), Beijing (3), Shanghai (2). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DYB
Manufacturer City Province Registered as Device types
Mehow Innovative (Huizhou) Ltd. Huizhou Guangdong Contract manufacturer 11
Tianjin Demax Medical Technology Co., Ltd. Tianjin Tianjin Contract manufacturer 5
Steris Sterilization Technologies (Suzhou) Ltd Suzhou Jiangsu Contract manufacturer 44
Shanghai INT Medical Instruments Co., Ltd. Shanghai Shanghai Contract manufacturer 10
Lepu Medical Technology (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7
Beijing Target Medical Technologies Inc. Beijing Beijing Contract manufacturer 7
Beijing Demax Medical Technology Co., Ltd. Beijing Beijing Manufacturer 5
Curatia Medical Limited Suzhou Jiangsu Specification developer 5
Tianjin Ethylene Oxide Sterilization Technology Co., Ltd. Tianjin Tianjin Contract manufacturer 4
Shanghai Microport EP Medtech Co., Ltd. Shanghai Shanghai Manufacturer 3
Becton Dickinson Medical Devices Co., Ltd. Suzhou Suzhou Jiangsu Contract manufacturer 2
Cardiocycle Medical(Suzhou) Co., Ltd. Suzhou Jiangsu Complaint-file establishment 1

Showing 12 of 13. All 13 manufacturers in China registered for Introducer, Catheter

Record

Regulatory record for Pounce Sheath
Listed by Surmodics, Inc., United States
FDA product code DYB
Device type Introducer, Catheter
Device class Class 2
Regulation 21 CFR 870.1340
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K231828
Record published 2023-09-21
Record revised 2025-07-02 (version 2)

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, manufacturing date

Catalogue Numbers

Catalogue numbers for Pounce Sheath
Catalogue number Size Status
PFS-0035-12F14 12Fr Introducer Sheath In distribution
PFS-0035-16F14 16 Fr Introducer Sheath In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Demax Beijing Demax Medical Technology Co., Ltd. 2,841
Arrow Teleflex Medical LLC 1,036
Prelude IDeal™ Merit Medical Systems, Inc. 294
Fast-Cath™ St. Jude Medical 213
Flexor Cook Incorporated 182
Prelude Ease™ Merit Medical Systems, Inc. 176
Performer Cook Incorporated 174
VSI Teleflex Medical LLC 154
Peel-Away Cook Incorporated 153
OptiSeal™ Greatbatch Medical 127
Brilliant Lepu Medical Technology (Beijing) Co., Ltd. 122
Super Sheath Togo Medikit Co., Ltd. 122

Showing 12 of 439. All products under Introducer, Catheter

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252227 2025-09-24
K231828 2023-09-07
K190644 2019-04-18

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