Endo Grasp
Catalogue number 173030, listed by Covidien LP, United States, under Forceps, Obstetrical. 2 manufacturers in China are registered for this product code.
2manufacturers in China registered for this device type
1catalogue number
Who Else Makes It
Concentrated in Jiangsu (1), Zhejiang (1). One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| B.Braun Medical (Suzhou) Co,.Ltd | Suzhou | Jiangsu | Contract manufacturer | 37 |
| Hangzhou Haizhu MIM Products Co., Ltd. | Hangzhou | Zhejiang | Exporter | 28 |
Record
| Listed by | Covidien LP, United States |
|---|---|
| FDA product code | HDA |
| Device type | Forceps, Obstetrical |
| Device class | Class 2 |
| Regulation | 21 CFR 884.4400 |
| 510(k) | K903205 |
| Record published | 2016-09-24 |
| Record revised | 2025-06-24 (version 8) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Storage | Handling environment temperature 0 to 120 °F |
| Packaging | Case of 6 |
| Sizes | Outer diameter 5 mm |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 173030 | Outer Diameter 5 mm | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Millennium | Avalign Technologies, Inc. | 40 |
| Novo Surgical | Novo Surgical, Inc. | 30 |
| Sklar® | Sklar Corporation | 20 |
| Hayden Medical | Hayden Medical Inc | 18 |
| Aesculap | Aesculap AG | 18 |
| Avalign | Avalign Technologies, Inc. | 17 |
| Ambler Surgical | Ambler Surgical, LLC | 14 |
| Pilling | Teleflex Medical LLC | 14 |
| Pilling | Avalign Technologies, Inc. | 11 |
| Integra® Jarit® | Integra LifeSciences Production Corporation | 11 |
| V. Mueller | Steris Corporation | 9 |
| Integra® Miltex® | Integra LifeSciences Production Corporation | 8 |
Showing 12 of 34. All products under Forceps, Obstetrical
Recalls Naming This Product
3 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Covidien | 510(k) number | 2019-03-13 | Class II | Process control | Sterilization method used was not consistent with the labeling and the approved sterilization method | 7248 units | 2020-04-23 |
| Covidien | 510(k) number | 2019-03-13 | Class II | Process control | Sterilization method used was not consistent with the labeling and the approved sterilization method | 240 units | 2020-04-23 |
| Covidien | 510(k) number | 2019-03-13 | Class II | Process control | Sterilization method used was not consistent with the labeling and the approved sterilization method | 148 units | 2020-04-23 |
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.