Aesculap
MILLS DUROGRIP TC Micro Needle Holder, straight, 8", (203 mm), with 0.2 mm pitch of serration, round handle, with ratchet, suture 6/0 - 10/0, non-sterile, reusable
Who Else Makes It
Concentrated in Zhejiang (4), Shanghai (1), Shandong (1). One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Beilun Plastech Inc | Ningbo | Zhejiang | Contract manufacturer | 13 |
| Shanghai Medical Instruments (Group) Ltd. Corp. | Shanghai | Shanghai | Contract manufacturer | 235 |
| Xinhua Surgical Instrument Co., Ltd. | Zibo | Shandong | Manufacturer | 222 |
| Huzhou Junda Industry Co., Ltd. | Anji | Zhejiang | Contract manufacturer | 129 |
| Hangzhou Kangji Medical Instrument Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 27 |
| Hangzhou Endo Medical Instrument Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 19 |
| Changzhou 3R Medical Device Technology Co., Ltd. | Changzhou | Jiangsu | Manufacturer | 16 |
| Auckland Medical Technology (Sichuan) Co., Ltd. | Luzhou | Sichuan | Manufacturer | 3 |
Record
| Listed by | Aesculap AG, Germany |
|---|---|
| FDA product code | HCF |
| Device type | Instrument, Ligature Passing And Knot Tying |
| Device class | Class 1 |
| Regulation | 21 CFR 878.4800 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| Premarket notification | Exempt |
| Record published | 2020-05-08 |
| Record revised | 2021-10-25 (version 3) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Prescription | Prescription only |
| Label carries | lot or batch number |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| MB116R | In distribution | |
| MG652R | In distribution | |
| MG530R | In distribution | |
| MG070R | In distribution | |
| MG912R | In distribution | |
| MG366R | In distribution | |
| FD046T | In distribution | |
| MG071R | In distribution | |
| MG649R | In distribution | |
| BM950R | In distribution | |
| MG911R | In distribution | |
| BM029R | In distribution | |
| MG005R | In distribution | |
| MG529R | In distribution | |
| MG536R | In distribution | |
| MB214R | In distribution | |
| MG535R | In distribution | |
| US126 | In distribution | |
| OM917R | In distribution | |
| MG538R | In distribution | |
| MG006R | In distribution | |
| MG537R | In distribution | |
| US131 | In distribution | |
| MB215R | In distribution | |
| MN217R | In distribution | |
| MB362R | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Boss Instruments | Boss Instruments, Ltd. | 360 |
| Elmed | Elmed, Inc. | 99 |
| MSI Precision Specialty Instruments | MED Saver, Inc. | 69 |
| Millennium | Avalign Technologies, Inc. | 53 |
| Castroviejo Needle Holder | Sontec Instruments, Inc. | 46 |
| Elmed Incorporated | Elmed, Inc. | 38 |
| Barraquer Needle Holder | Sontec Instruments, Inc. | 23 |
| Wexler Surgical, Inc. | Wexler Surgical, Inc. | 20 |
| Gimmi | Gimmi Gmbh | 16 |
| Marina Medical | Marina Medical Instruments, Inc. | 16 |
| Weck | Teleflex Medical LLC | 12 |
| Novo Surgical | Novo Surgical, Inc. | 11 |
Showing 12 of 156. All products under Instrument, Ligature Passing And Knot Tying
Recalls
2 of these are 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.
| Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|
| 2023-12-29 | Class II | Nonconforming Material/Component | Needle Holder MB215R was inadvertently distributed as MB362R. Similarly, MB362R was distributed as MB215R during the affected distribution date range. The issue may lead to a short delay in procedure. | 60 |
| 2023-12-29 | Class II | Nonconforming Material/Component | Needle Holder MB215R was inadvertently distributed as MB362R. Similarly, MB362R was distributed as MB215R during the affected distribution date range. The issue may lead to a short delay in procedure. | 53 |
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.