| Primary Device ID | 06939282438536 |
| NIH Device Record Key | 9eda0118-7830-42c5-b46a-728c6c5ef7ab |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Circular Stapler |
| Version Model Number | FCSSWAE34 |
| Company DUNS | 559966539 |
| Company Name | B. J. ZH. F. Panther Medical Equipment Co., Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06939282438536 [Primary] |
| GDW | Staple, Implantable |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[06939282438536]
Ethylene Oxide
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-05-07 |
| Device Publish Date | 2018-04-04 |
| 06939282448740 | FCSME34 |
| 06939282448733 | FCSME32 |
| 06939282448726 | FCSME29 |
| 06939282448719 | FCSME26 |
| 06939282448702 | FCSME24 |
| 06939282438611 | FCSSME34 |
| 06939282438604 | FCSSME33 |
| 06939282438598 | FCSSME32 |
| 06939282438581 | FCSSME31 |
| 06939282438574 | FCSSWBE34 |
| 06939282438567 | FCSSWBE33 |
| 06939282438550 | FCSSWBE32 |
| 06939282438543 | FCSSWBE31 |
| 06939282438536 | FCSSWAE34 |
| 06939282438529 | FCSSWAE33 |
| 06939282438512 | FCSSWAE32 |
| 06939282438505 | FCSSWAE31 |
| 06939282418606 | FCSLWBE21 |
| 06939282418590 | FCSLWBE34 |
| 06939282418583 | FCSLWBE32 |
| 06939282418576 | FCSLWBE29 |
| 06939282418569 | FCSLWBE26 |
| 06939282418552 | FCSLWBE24 |