Memmen Punch
Catalogue number AE-8305, listed by Katena Products, Inc., United States, under Punch, Corneo-Scleral. 3 manufacturers in China are registered for this product code.
3manufacturers in China registered for this device type
1catalogue number
Who Else Makes It
Concentrated in Jiangsu (2), Shanghai (1). One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Malosa Medical Instruments (Changshu) Limited | Changshu | Jiangsu | Contract manufacturer | 24 |
| Shanghai Medical Instruments (Group) Ltd. Corp. | Shanghai | Shanghai | Contract manufacturer | 235 |
| Sihong Ophsurin Co., Ltd. | Suqian | Jiangsu | Manufacturer | 17 |
Record
| Listed by | Katena Products, Inc., United States |
|---|---|
| FDA product code | HNJ |
| Device type | Punch, Corneo-Scleral |
| Device class | Class 1 |
| Regulation | 21 CFR 886.4350 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2022-12-07 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| AE-8305 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| ONE | Moria, Inc. | 46 |
| MSI Precision Specialty Instruments | MED Saver, Inc. | 33 |
| Moria | Moria, Inc. | 18 |
| Punches | Aurora Surgical, LLC | 14 |
| Ambler Surgical | Ambler Surgical, LLC | 8 |
| Trab. Punch | Katena Products, Inc. | 7 |
| Millennium | Avalign Technologies, Inc. | 7 |
| Punch, Corneo-Scleral | Geuder Aktiengesellschaft | 6 |
| Trabeculotome | Aurora Surgical, LLC | 6 |
| Rumex | Rumex International Co. | 5 |
| Stephens Instruments | Krishna Imports Inc | 5 |
| V. Mueller | Steris Corporation | 3 |
Showing 12 of 33. All products under Punch, Corneo-Scleral
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.