SEARCH RESULTS FOR: 代办AT(7976 results)
Single-Use Surgical Tool
Med-El Elektromedizinische Geräte Gesellschaft m.b.H.
33056
In Commercial Distribution
- 09008737330569 ()
- Surgical implant template, single-use
Single-Use Surgical Tool
Med-El Elektromedizinische Geräte Gesellschaft m.b.H.
36894
In Commercial Distribution
- 09008737368944 ()
- Surgical implant template, single-use
The Cross-Seal Device is composed of a Catheter, Suture Delivery System, and Handle.
The Cross-Seal Device tracks over a standard 0.038” or 0.035” (minimum length 130 cm) guidewire. A hemostasis valve located in the middle of the CATHETER limits blood flow from the GUIDEWIRE PORT through the CATHETER with or without the guidewire in place. The SUTURE DELIVERY SYSTEM contains NEEDLES, LOCATOR WINGS, and the NEEDLE BARREL that control suture placement around the arteriotomy. The HANDLE contains the SLIDER, BLEEDING INDICATOR, PLUNGER, RESET 1 BUTTON (SLIDER RETRACTOR), and RESET 2 BUTTON (LOCATOR WINGS RETRACTOR). The SLIDER triggers a mechanism that opens the LOCATOR WINGS and creates a sandwich configuration to stabilize the delivery system within the vessel wall. The BLEEDING INDICATOR connects to a lumen that has an intraluminal port positioned at the distal end of the Suture Delivery System to allow bleeding back to ensure Suture Delivery System is positioned properly in the femoral artery. The NEEDLE BARREL keeps the Cross-Seal Device from moving deeper inside the vessel, stabilizes the device once the LOCATOR WINGS are opened and retrieves the disengaged suture-carried NEEDLES. The PLUNGER triggers the NEEDLES to deploy sutures and simultaneously close the LOCATOR WINGS. The GUIDEWIRE GUIDE is the feature at distal handle portion which allows physician to practice coaxial insertion of device along guidewire if necessary.
MEDEON BIODESIGN, INC.
002
In Commercial Distribution
- 04719872920359 ()
- 04719872920366 ()
- 04719872920373 ()
002
- Polyolefin/fluoropolymer suture, monofilament
Approval for the use of t-cell xtend reagent with the t-spot. Tb test, in order to extend the time from sample collection to sample processing from within 8 hours of venipuncture to between 23 and 30 hours post venipuncture; and to make a technical correction to the t-spot. Tb test package insert to change the number of blood collection tubes required from (2) 6 ml heparin tubes to (1) 6 ml heparin tube. The t-cell xtend reagent is indicated for use with the t-spot. Tb test for the pre-treatment of whole blood prior to lymphocyte separation. The reagent aids in the removal of selected white blood cells from whole blood stored at room temperature (18-25 degrees c).
Oxford Immunotec, Inc.
TTK.650
In Commercial Distribution
- 15051716000053 ()
TTK.650US
- Cell centrifugation/density gradient separation reagent IVD
Approval for the use of t-cell xtend reagent with the t-spot. Tb test, in order to extend the time from sample collection to sample processing from within 8 hours of venepuncture to between 23 and 30 hours post venepuncture; and to make a technical correction to the t-spot. Tb test package insert to change the number of blood collection tubes required from (2) 6 ml heparin tubes to (1) 6 ml heparin tube. The t-cell xtend reagent is indicated for use with the t-spot. Tb test for the pre-treatment of whole blood prior to lymphocyte separation. The reagent aids in the removal of selected white blood cells from whole blood stored at room temperature (18-25 degrees c).
Oxford Immunotec, Inc.
TTK.610
In Commercial Distribution
- 15051716000022 ()
TTK.610US
- Cell centrifugation/density gradient separation reagent IVD
No Description
MEDINOL LTD.
LUN400R38US
Not in Commercial Distribution
- 07290107014595 ()
- Length: 38 Millimeter
- Lumen/Inner Diameter: 4.0 Millimeter
- Drug-eluting coronary artery stent, non-bioabsorbable-polymer-coated
No Description
MEDINOL LTD.
LUN350R38US
Not in Commercial Distribution
- 07290107014588 ()
- Length: 38 Millimeter
- Lumen/Inner Diameter: 3.5 Millimeter
- Drug-eluting coronary artery stent, non-bioabsorbable-polymer-coated
No Description
MEDINOL LTD.
LUN300R38US
Not in Commercial Distribution
- 07290107014571 ()
- Length: 38 Millimeter
- Lumen/Inner Diameter: 3.0 Millimeter
- Drug-eluting coronary artery stent, non-bioabsorbable-polymer-coated
No Description
ACRE PHARMA LIMITED
N/A
In Commercial Distribution
- 05060604130065 ()
- Synovial fluid supplementation medium
"One box of RHA® 3 contains two blisters and one instruction for use.
Each blister contains a 1mL prefilled syringe and two needles (27G 1/2).
Box Packaging (ID 07640173234159) is defined as unit of sales and identified with a serial number."
Teoxane SA
RHA® 3 US 1ml Schott/2 aig. TSK 27G1/2
In Commercial Distribution
- 07640173234241 ()
940008/03
- Dermal tissue reconstructive material, microbe-derived, anaesthetic