What is FDA product code QEH?

A neuraxial piston syringe is intended to inject or withdraw fluid from the neuraxial space with neuraxial specific connections. This product code may include epidural, peripheral, subarachnoid/spinal block, intrathecal and/or intracerebroventricular administration routes. The connector for neuraxial applications is intended to facilitate ANSI/AAMI/ISO 80369-6:2016 compliant neuraxial specific connections.

Caina · Piston Syringe with Neuraxial Connector Epidural, Peripheral, And/Or Indirect Cerebral Spinal Fluid Contact → General Hospital

Name: Caina
Brand: Caina

1manufacturer

1catalogue number

1510(k) clearance

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code QEH
Manufacturer	City	Province	Registered as	Device types
Jiangsu Caina Medical Co., Ltd.	Jiangyin	Jiangsu	Contract manufacturer	20

Record

Regulatory record for Caina
Listed by	Jiangsu Caina Medical Co., Ltd., China
FDA product code	QEH
Device type	Piston Syringe With Neuraxial Connector Epidural, Peripheral, And/Or Indirect Cerebral Spinal Fluid Contact
Device class	Class 2
Regulation	21 CFR 880.5860
Establishment	Contract manufacturer, Manufacturer, Exporter
510(k)	K181374
Record published	2026-04-14

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Supplied sterile	Yes
Single use	Yes
Prescription	Prescription only
Latex	Labelled latex-free
Label carries	lot or batch number, expiry date, manufacturing date
Packaging	Pack of 10, pack of 180

Catalogue Numbers

Catalogue numbers for Caina
Catalogue number	Size	Status
1mL		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
BD Syringe NRFit™ Lok	Becton, Dickinson AND Company	5
BD Syringe NRFit™ Slip	Becton, Dickinson AND Company	3
Female NRFit Tip Cap	Tech Industries. Inc.	1

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K181374	2018-12-14

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.

Caina