Primary Device ID | 10841268109688 |
NIH Device Record Key | 7a8f776b-28d4-4b8f-99ac-688aeea89cd6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Guidewire |
Version Model Number | SGW-070-72 |
Catalog Number | SGW-070-72 |
Company DUNS | 943156836 |
Company Name | GALT MEDICAL CORP. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Outer Diameter | 0.018 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841268109681 [Primary] |
GS1 | 10841268109688 [Package] Contains: 00841268109681 Package: Shelf Box [5 Units] In Commercial Distribution |
GS1 | 20841268109685 [Package] Package: Shipper Box [50 Units] In Commercial Distribution |
DQX | Wire, Guide, Catheter |
Steralize Prior To Use | true |
Device Is Sterile | true |
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
[10841268109688]
Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-11-08 |
Device Publish Date | 2021-10-29 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GUIDEWIRE 87540652 5401314 Live/Registered |
Guidewire Software, Inc. 2017-07-24 |
GUIDEWIRE 78662211 3185991 Live/Registered |
Guidewire Software, Inc. 2005-06-30 |
GUIDEWIRE 77016329 3273576 Dead/Cancelled |
Yu, Steven S. 2006-10-07 |
GUIDEWIRE 76474094 not registered Dead/Abandoned |
GUIDEWIRE SYSTEMS, INC. 2002-12-12 |