SEARCH RESULTS FOR: 得克萨斯A(3710369 results)

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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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n/a - 00874750007240

3813 HTD PNT 35OD, SIL P-TAPS
HANS RUDOLPH, INC.
3813
Not in Commercial Distribution

  • 00874750007240 ()
113463

  • Pneumotachograph

n/a - 00874750007233

3700 PNT 22LG/35SM, SIL P-TAPS
HANS RUDOLPH, INC.
3700
Not in Commercial Distribution

  • 00874750007233 ()
113462

  • Pneumotachograph

N/A - 00874750007226

8311 PNT 22/15 SM & LG FLANGE
HANS RUDOLPH, INC.
8300
Not in Commercial Distribution

  • 00874750007226 ()
113409

  • Pneumotachograph

n/a - 00874750007219

4700 NONHTD PNT CUSTOM FLG'S
HANS RUDOLPH, INC.
4700
Not in Commercial Distribution

  • 00874750007219 ()
113225

  • Pneumotachograph

n/a - 00874750007202

2600 2W NRBV MPORT SMC FLOWMTR
HANS RUDOLPH, INC.
2600
Not in Commercial Distribution

  • 00874750007202 ()
113201

  • Non-rebreathing valve, reusable

n/a - 00874750007196

HH PNT SGL SCR CONSENTIUS TECH
HANS RUDOLPH, INC.
3813
Not in Commercial Distribution

  • 00874750007196 ()
113183

  • Pneumotachograph

n/a - 00874750007189

ELEV FIO2/2600 PER SMC SPEC
HANS RUDOLPH, INC.
2600
Not in Commercial Distribution

  • 00874750007189 ()
113138

  • Non-rebreathing valve, reusable

n/a - 00874750007172

3830C PNT/HTR SHELL/1.375OD 2X
HANS RUDOLPH, INC.
3830
Not in Commercial Distribution

  • 00874750007172 ()
113120

  • Pneumotachograph

n/a - 00874750007165

2700 W/FELUER/1.18 EXH/2X 6-32
HANS RUDOLPH, INC.
2700
Not in Commercial Distribution

  • 00874750007165 ()
113096

  • Non-rebreathing valve, reusable

n/a - 00874750007158

3700 OEM PNT HTD 22 LG/ 35 SM
HANS RUDOLPH, INC.
3700
Not in Commercial Distribution

  • 00874750007158 ()
113059

  • Pneumotachograph
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