Busse Hospital Disposable
4.5MM Pellet Insertion Tray with Medium Gloves
1manufacturer
1catalogue number
Who Else Makes It
Registered in Zhejiang.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Hangzhou Endo Medical Instrument Co., Ltd. | Hangzhou | Zhejiang | Contract manufacturer | 19 |
Record
| Listed by | Robert Busse & Co., Inc., United States |
|---|---|
| FDA product code | FBQ |
| Device type | Trocar, Gastro-Urology |
| Device class | Class 2 |
| Regulation | 21 CFR 876.5090 |
| Premarket notification | Exempt |
| Record published | 2020-07-17 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Latex | Labelled latex-free |
| Label carries | lot or batch number, expiry date |
| Packaging | Pack of 20 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| B1362 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Busse Hospital Disposables | Robert Busse & Co., Inc. | 62 |
| Riwo-ART | Richard Wolf Gmbh | 52 |
| Trocar, Gastro-Urology | Richard Wolf Gmbh | 43 |
| Doctor Nice | B. ALI Impex | 23 |
| MIP Minimal Invasive Pcnl | Karl Storz GmbH & Co. KG | 6 |
| Spring Grip | Covidien LP | 6 |
| Integra® Miltex® | Integra LifeSciences Production Corporation | 6 |
| Trotec | Richard Wolf Gmbh | 6 |
| Trocar, Gastro-Urology | Karl Storz GmbH & Co. KG | 5 |
| Cook | Cook Incorporated | 5 |
| EchoTip | Cook Incorporated | 3 |
| Strauss Surgical | American Medical Endoscopy | 3 |
Showing 12 of 19. All products under Trocar, Gastro-Urology
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 | Closed |
|---|---|---|---|---|---|---|---|
| Busse Hospital Disposables | UDI-DI | 2022-02-22 | Class II | Other | Busse Convenience kits contain one or more swab/swabstick drug products, manufactured by Professional Disposables International (PDI), that are subject to a drug recall due to uncertainty of the adequacy of the validation of the test method | 30 units | 2024-04-17 |
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.