Primary Device ID | 06939282418583 |
NIH Device Record Key | 12d92ec6-9aa6-4cfc-bad1-6d89852e4600 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Circular Stapler |
Version Model Number | FCSLWBE32 |
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 | 06939282418583 [Primary] |
GDW | Staple, Implantable |
Steralize Prior To Use | true |
Device Is Sterile | true |
[06939282418583]
Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-04-19 |
Device Publish Date | 2018-03-19 |
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 |