Primary Device ID | 10841962109649 |
NIH Device Record Key | 4ff92ca4-695c-4db6-8757-66c8d5acef89 |
Commercial Distribution Discontinuation | 2017-03-16 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | X-Trans™ 24" Double Armboard |
Version Model Number | 8002067 |
Catalog Number | 8002067 |
Company DUNS | 808875397 |
Company Name | Qfix |
Device Count | 1 |
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 | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com | |
Phone | +1(610)268-0585 |
Compliance@qfix.com |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Size Text, specify | 0 |
Width | 24 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10841962109649 [Primary] |
GDC | TABLE, OPERATING-ROOM, ELECTRICAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-12-11 |
Device Publish Date | 2016-12-22 |
10841962107386 - Aquaplast PS™ | 2023-12-11 Blush, 1/16" - 3" x 3" Nasal Splint Blanks |
10841962107409 - Aquaplast PS™ | 2023-12-11 Blush, 1/16" Small Silver splint, pkg. of 10 |
10841962107423 - Aquaplast PS™ | 2023-12-11 Blush, 1/16" Large Silver splint, pkg. of 10 |
10841962107447 - Aquaplast PS™ | 2023-12-11 Blush, 1/16" Tie Down Dressings, 6" x 9" sheet |
10841962107461 - Aquaplast PS™ | 2023-12-11 Blush, 1/16", Trapezoidal Nasal Splint, pkg. of 10 |
10841962107485 - Aquaplast PS™ | 2023-12-11 Blush, 1/16", Trapezoidal Nasal Splints |
10841962107492 - Aquaplast PS™ | 2023-12-11 Blush, 3/32", 3 x 3" Nasal Splint Blanks |
10841962107515 - Aquaplast PS™ | 2023-12-11 Blush, 3/32", 18" x 24" sheet |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
X-TRANS 79263488 not registered Live/Pending |
FUJIFILM Corporation 2019-05-22 |