Tevadaptor Syringe Adaptor Lock

for use with OnGuard CSTD containing Tevadaptor Drug Reconstitution and Administration Components

Registry build 21.09.26
1manufacturer
1catalogue number
6510(k) clearances naming this product code
1recall

Who Else Makes It

Registered in Shandong.

Chinese manufacturers registered for FDA product code ONB
Manufacturer City Province Registered as Device types
Shandong Ande Healthcare Apparatus Co., Ltd. Zibo Shandong Manufacturer 7

Record

Regulatory record for Tevadaptor Syringe Adaptor Lock
Listed by Simplivia Healthcare Ltd., Israel
FDA product code ONB
Device type Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System
Device class Class 2
Regulation 21 CFR 880.5440
Establishment Manufacturer
Record published 2021-02-18
Record revised 2024-03-29 (version 3)

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, serial number
Packaging Pack of 6
Distribution end date 2024-03-01

Catalogue Numbers

Catalogue numbers for Tevadaptor Syringe Adaptor Lock
Catalogue number Size Per pack Status
412126 50 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
ICU Medical ICU Medical, Inc 255
Equashield Equashield Medical Ltd 83
BD PhaSeal BD Switzerland Sàrl 23
Halo J & J Solutions, Inc. 14
ProSeal Cstd Epic International (Thailand) Co., Ltd. 12
BD PhaSeal Optima BD Switzerland Sàrl 11
Equashield Cstd Equashield Medical Ltd 6
Luer Lock Adaptor 2 Swivel A Equashield Medical Ltd 1
ICU Medical, Inc. ICU Medical, Inc 1
OnGuard®2 Cstd Luer Lock Adaptor Simplivia Healthcare Ltd. 1
OnGuard2 Syringe Adaptor, 5 Units Simplivia Healthcare Ltd. 1
OnGuard 2 Cstd Bag Adaptor LL with Ultrasite Simplivia Healthcare Ltd. 1

Showing 12 of 60. All products under Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253033 2025-10-21
K251411 2025-08-05
K231286 2023-08-02
K210707 2021-09-23
K201142 2021-02-25
K192866 2020-05-07

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2022-03-08 Class II Equipment maintenance Disconnection of the OnGuard2 Bag Adaptor SP from infusion bags which may result in spillage of hazardous medications. 293,520

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