Verify
Brush for VERIFY RESI-TEST Endo Protein Detection Cleaning Indicator, Large is designed to detect a broad spectrum of protein residues and is intended for use after manual or automated…
Brush for VERIFY RESI-TEST Endo Protein Detection Cleaning Indicator, Large is designed to detect a broad spectrum of protein residues and is intended for use after manual or automated cleaning and prior to high level disinfection or sterilization.
Who Else Makes It
Concentrated in Jiangsu (20), Zhejiang (8), Guangdong (6). 8 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Zhejiang Chuangxiang Medical Technology Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 27 |
| Yangzhou Fartley Medical Instrument Technology Co., Ltd. | Yangzhou | Jiangsu | Contract manufacturer | 24 |
| Suzhou Jingle Polymer Medical Apparatus Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 19 |
| Hangzhou Aosi Healthcare Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 18 |
| Suzhou Suning Underpad Co., Ltd. | Suzhou, Jiangsu Province | Contract manufacturer | 11 | |
| Jiangsu Power-Endo Medical Technology Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 7 |
| Xinle Huabao Medical Products Co., Ltd. | Xinle | Hebei | Contract manufacturer | 2 |
| Dongguan Liangyou Electronic Technology Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 1 |
| Boen Healthcare Co., Ltd. | Suzhou | Jiangsu | Specification developer | 263 |
| Ningbo Tianbo First AID Product Co., Ltd. | Ningbo | Zhejiang | Repacker / relabeller | 66 |
| Dongguan City Ruimi Gift Products Co Ltd | Dongguan | Guangdong | Repacker / relabeller | 62 |
| Micro-Tech (Nanjing) Co., Ltd. | Nan Jing | Jiangsu | Contract manufacturer | 49 |
Showing 12 of 43. All 43 manufacturers in China registered for Accessories, Cleaning Brushes, For Endoscope
Record
| Listed by | Steris Corporation, United States |
|---|---|
| FDA product code | MNL |
| Device type | Accessories, Cleaning Brushes, For Endoscope |
| Device class | Class 1 |
| Regulation | 21 CFR 876.1500 |
| Establishment | Contract manufacturer, Contract steriliser, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| Premarket notification | Exempt |
| Record published | 2022-09-23 |
| Record revised | 2025-04-11 (version 3) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Single use | Yes |
| Over the counter | Yes |
| Label carries | lot or batch number, expiry date, manufacturing date |
| Packaging | Case of 4, box of 25, case of 2 |
| Distribution end date | 2025-04-10 |
Catalogue Numbers
| Catalogue number | Size | Per pack | Status |
|---|---|---|---|
| Resi-Test | 25 | In distribution | |
| LCC101 | 25 | Withdrawn | |
| Resi-Test | Withdrawn | ||
| Resi-Test | 25 | Withdrawn | |
| Resi-Test | 25 | Withdrawn | |
| Resi-Test | Withdrawn | ||
| Resi-Test | 50 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Endo Carry-On Procedure Kit | Medivators Inc | 1,263 |
| Custom Procedure Kit | Medivators Inc | 433 |
| Compliance EndoKit™ | Boston Scientific Corporation | 404 |
| Trial Procedure Kit | Medivators Inc | 403 |
| Accessories, Cleaning Brushes, For Endoscope | Steris Corporation | 174 |
| Key Surgical Endoscope Brushes | Key Surgical, LLC | 121 |
| Accessories, Cleaning Brushes, For Endoscope | Key Surgical, LLC | 97 |
| Cygnus | Aspen Surgical Products, Inc. | 56 |
| Accessories, Cleaning Brushes, For Endoscope | Karl Storz GmbH & Co. KG | 49 |
| 9000 Series Disposable Channel Cleaning Brush | Primed Instruments, Inc. | 47 |
| Medline | Medline Industries, Inc. | 45 |
| Endoscope Brushes | Healthmark Industries Co., Inc. | 34 |
Showing 12 of 465. All products under Accessories, Cleaning Brushes, For Endoscope
Recalls Naming This Product
1 recall names this product by its own identifier, the UDI on its label.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| Mckesson Medical-Surgical Inc. Corporate Office | UDI-DI | 2024-01-09 | Class II | Storage | Facility Critical Temperature Excursions on 08-JAN 2024 in Walk-In refrigerator due to mechanical failures, causing temperatures to fall below the validated range of 35.6 – 46.4 Degrees Fahrenheit (2 – 8 Degrees Celsius) for up to 60 minute | 25 units |
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.