MetriCide OPA Plus

orthoPhthalaldehyde Solution high level disinfectant for semicritical medical devices

Registry build 21.09.26
1manufacturer
1catalogue number
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 MED
Manufacturer City Province Registered as Device types
Saint-Gobain Life Sciences (Hangzhou) Co., Ltd. Hangzhou Zhejiang Contract manufacturer 5

Record

Regulatory record for MetriCide OPA Plus
Listed by Metrex Research, United States
FDA product code MED
Device type Sterilant, Medical Devices
Device class Class 2
Regulation 21 CFR 880.6885
Establishment Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2016-08-31
Record revised 2023-04-04 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Over the counter Yes
Label carries lot or batch number, expiry date
Storage Special storage condition: Store original sealed containers at a controlled room temperature of 15 – 30
Packaging Case of 4
Sizes Total volume 1 Gallon

Catalogue Numbers

Catalogue numbers for MetriCide OPA Plus
Catalogue number Size Status
10-6000 Total Volume 1 Gallon In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Sterilant, Medical Devices Steris Corporation 149
Formed Irrigating Cystotomes Sterimedix Ltd. 37
Hydrodissection Cannulae Sterimedix Ltd. 29
Sterilant, Medical Devices Corporation Steris Canada 29
Anterior Chamber Maintenance Cannulae Sterimedix Ltd. 17
Anaesthetic Needles Sterimedix Ltd. 14
Formed Capsularhexis Cystotomes Sterimedix Ltd. 8
Refractive Cannulae Sterimedix Ltd. 8
enspire Corporation Steris Canada 8
Cidex™ Advanced Sterilization Products Services Inc. 8
Bimanual Cannulae and Hand Pieces Sterimedix Ltd. 7
Bimanual I/A Systems Sterimedix Ltd. 7

Showing 12 of 96. All products under Sterilant, Medical Devices

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K931592 1994-12-06
K930284 1994-12-06
K931052 1994-12-06

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