SEARCH RESULTS FOR: 外链资源优化程序方法👉TG@yuantou2048👈谷歌外链发布10万条(3732 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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Zenith Renu - 10827002433646

Zenith Renu, AAA Ancillary Graft Main Body Extension
COOK INCORPORATED
G43364
In Commercial Distribution

  • 10827002433646 ()
RX1-36-100

  • Synthetic vascular graft

Zenith Renu - 10827002433639

Zenith Renu, AAA Ancillary Graft Main Body Extension
COOK INCORPORATED
G43363
In Commercial Distribution

  • 10827002433639 ()
RX1-36-77

  • Synthetic vascular graft

Zenith Renu - 10827002433622

Zenith Renu, AAA Ancillary Graft Main Body Extension
COOK INCORPORATED
G43362
In Commercial Distribution

  • 10827002433622 ()
RX1-36-54

  • Synthetic vascular graft

Hancock™ 150 - 00763000926472

HANCOCK VALVED CONDUIT MO 14MM
MEDTRONIC, INC.
HC150-14
In Commercial Distribution

  • 00763000926472 ()

  • 14 MM


  • Synthetic vascular graft

Hancock™ 150 - 00763000926465

HANCOCK VALVED CONDUIT MO 12MM
MEDTRONIC, INC.
HC150-12
In Commercial Distribution

  • 00763000926465 ()

  • 12 MM


  • Synthetic vascular graft

SJM™ - 05414734500920

No Description
ST. JUDE MEDICAL, INC.
3617
In Commercial Distribution

  • 05414734500920 ()
3617

  • Electrocardiographic electrode, single-use

SJM™ - 05414734506373

No Description
ST. JUDE MEDICAL, INC.
EX3000
In Commercial Distribution

  • 05414734506373 ()
EX3000

  • Electrocardiographic electrode, single-use

Access AFP - H628332111

The Access AFP assay is a paramagnetic particle, chemiluminescent immunoassay for use with the Access Immunoassay Systems for the quantitative determination of alpha-fetoprotein (AFP) in: 1. Human serum, as an aid in the management of patients with non-seminomatous testicular cancer. 2. Maternal serum and amniotic fluid at 15 to 20 weeks gestation, to aid in the detection of fetal open neural tube defects (ONTD). Test results, when used in conjunction with ultrasonography, are safe and effective aids in the detection of fetal ONTD. The assay is intended for use in conjunction with other diagnostic tools such as ultrasound and amniography.
Beckman Coulter, Inc.
33211
In Commercial Distribution

  • H628332111 ()
33211

  • Trisomy 21-risk hormone IVD, kit, chemiluminescent immunoassay

Vysis - 00884999042773

Vysis ALK Break Apart FISH Probe Kit
ABBOTT MOLECULAR INC.
06N38-053
In Commercial Distribution

  • 00884999042773 ()
06N38-053

  • Anaplastic lymphoma kinase (ALK) genetic mutation IVD, probe

Vysis - 00884999042728

Vysis ALK Break Apart FISH Probe Kit
ABBOTT MOLECULAR INC.
06N38-033
In Commercial Distribution

  • 00884999042728 ()
06N38-033

  • Anaplastic lymphoma kinase (ALK) genetic mutation IVD, probe
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