PNEUMOSTOP® 110200
GUDID 10850200006749
PNEUMOSTOP® DEVICE Each sterile pouch contains one single patient use PNEUMOSTOP® DEVICE.
LSI Solutions, Inc.
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| NIH Device Record Key | a2bba140-9cc5-4f00-a96b-5105b2f5e7a3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PNEUMOSTOP® |
| Version Model Number | 110200 |
| Catalog Number | 110200 |
| Company DUNS | 603420183 |
| Company Name | LSI Solutions, Inc. |
| Device Count | 3 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
| Length | 2.5 Inch |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850200006742 [Primary] |
| GS1 | 10850200006749 [Package] Contains: 00850200006742 Package: Inner pack [6 Units] In Commercial Distribution |
| GS1 | 40850200006740 [Unit of Use] |
FDA Product Code
| NWW | Hysteroscope accessories |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
[10850200006749]
Ethylene Oxide
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-13 |
| Device Publish Date | 2020-07-03 |
On-Brand Devices [PNEUMOSTOP®]
| 10850200006756 | PNEUMOSTOP® PLUS DEVICE Each sterile pouch contains one single patient use PNEUMOSTOP® PLUS DE |
| 10850200006749 | PNEUMOSTOP® DEVICE Each sterile pouch contains one single patient use PNEUMOSTOP® DEVICE. |
| 10850012846014 | PNEUMOSTOP® PLUS DEVICE |
| 10850012846007 | PNEUMOSTOP® DEVICE |
Trademark Results [PNEUMOSTOP]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PNEUMOSTOP 86024532 4598672 Live/Registered |
LSI SOLUTIONS, INC. 2013-07-31 |
 PNEUMOSTOP 74173304 1691554 Live/Registered |
BLOHM + VOSS INDUSTRIES GMBH 1991-06-06 |
 PNEUMOSTOP 73450042 1363355 Dead/Cancelled |
HOWALDTSWERKE - DEUTSCHE WERFT 1983-10-27 |
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