Centurion
Sterile Magill Forcep 6 3/4' (MAGF634)
2manufacturers in China registered for this device type
5catalogue numbers in this listing
Who Else Makes It
Concentrated in Shanghai (1), Shandong (1).
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Shanghai Medical Instruments (Group) Ltd. Corp. | Shanghai | Shanghai | Contract manufacturer | 235 |
| Xinhua Surgical Instrument Co., Ltd. | Zibo | Shandong | Manufacturer | 222 |
Record
| Listed by | Centurion Medical Products Corporation, United States |
|---|---|
| FDA product code | BWB |
| Device type | Forceps, Tube Introduction |
| Device class | Class 1 |
| Regulation | 21 CFR 868.5780 |
| Premarket notification | Exempt |
| Record published | 2022-01-01 |
| Record revised | 2023-01-16 (version 2) |
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 |
| Packaging | Case of 20 |
| UDI direct marking | Exempt |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| I67985 | In distribution | |
| I67985 | In distribution | |
| 67575 | In distribution | |
| I67985 | In distribution | |
| 67575 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Novo Surgical Inc. | Novo Surgical, Inc. | 8 |
| Novo Surgical | Novo Surgical, Inc. | 7 |
| AincA® | Anesthesia Associates, Inc. | 7 |
| BR Surgical, LLC | BR Surgical LLC | 6 |
| V. Mueller | Steris Corporation | 6 |
| Instrapac | Robinson Healthcare Limited | 5 |
| Medicon | Medicon eG. Chirurgiemechaniker-Genossenschaft | 5 |
| Wexler Surgical, Inc. | Wexler Surgical, Inc. | 4 |
| Integra® Miltex® | Integra LifeSciences Production Corporation | 4 |
| Eco Magill | Timesco Healthcare Ltd | 3 |
| Quinelato | Schobell Industrial Ltda | 3 |
| Boss Instruments | Boss Instruments, Ltd. | 3 |
Showing 12 of 16. All products under Forceps, Tube Introduction
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 |
|---|---|---|---|---|---|---|
| Medline Industries, LP – Northfield | UDI-DI | 2024-02-23 | Class II | Process control | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. | 480 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.