SEARCH RESULTS FOR: 【溦信88931766】i换脸张子枫11V4G最全所有视频资源全部作品合集.ldb(15744 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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Manual & CDs, APLS IgM IFU, SW4.1_v1
BIO-RAD LABORATORIES, INC.
SW4.1V1
In Commercial Distribution

  • 00847865012980 ()

  • 1 Each
6652065B

  • Phospholipid antibody IVD, kit, multiplex
APLS IgG, IgM and IgA Assay Protocol File CD, SW4.1_v1 US Only
BIO-RAD LABORATORIES, INC.
SW4.1V1
In Commercial Distribution

  • 00847865012973 ()

  • 1 Each
6651975B

  • Phospholipid antibody IVD, kit, multiplex
Manual & CDs, APLS IgG IFU, SW4.1_v1, US Only
BIO-RAD LABORATORIES, INC.
SW4.1V1
In Commercial Distribution

  • 00847865012966 ()

  • 1 Each
6651965B

  • Phospholipid antibody IVD, kit, multiplex
Manual & CDs, BioPlex 2200 APLS IgG IFU, SW4_v1, US Only
BIO-RAD LABORATORIES, INC.
SW4_1
In Commercial Distribution

  • 00847865012522 ()

  • 1 Each
6651965A

  • Phospholipid antibody IVD, kit, multiplex
Manual & CDs, APLS IgM IFU, SW4_v1, US Only
BIO-RAD LABORATORIES, INC.
SW4_1
In Commercial Distribution

  • 00847865012515 ()

  • 1 Each
6652065A

  • Phospholipid antibody IVD, kit, multiplex
APLS IgG, IgM and IgA Assay Protocol File CD, SW4_v1
BIO-RAD LABORATORIES, INC.
SW4_1
In Commercial Distribution

  • 00847865012508 ()

  • 1 Each
6651975A

  • Phospholipid antibody IVD, kit, multiplex
Manual & CDs, APLS IgA IFU, SW4_v1, US Only
BIO-RAD LABORATORIES, INC.
SW4_1
In Commercial Distribution

  • 00847865002998 ()

  • 1 Each
6652165A

  • Phospholipid antibody IVD, kit, multiplex
APLS IgA Reagent Pack
BIO-RAD LABORATORIES, INC.
6652150
In Commercial Distribution

  • 00847865000710 ()

  • 100 Tests
6652150

  • Phospholipid antibody IVD, kit, multiplex
The CarePath system facilitates evaluations measuring urine output. It consists of the CarePath device, accompanying documents, and training. The system: • Measures and calculates flow rate and volume from urination data • Automatically transmits urination data to a secure location • Creates and provides uroflow reports to healthcare providers The intended operator of the CarePath device is the patient. The CarePath system has no user-serviceable components. This system is not to be serviced or maintained by the user. The intended environments are hospitals, clinics, doctor’s offices and the patient’s home.
I/O Urology Corp.
DCDUFD-001M
In Commercial Distribution

  • 00860010862209 ()


  • Urine flowmeter, reusable
Stop Solution
IMMCO DIAGNOSTICS, INC.
2310
In Commercial Distribution

  • 00845714002793 ()

  • 12 ml
2310

  • Multiple antinuclear antibody (ANA) screening IVD, kit, enzyme immunoassay (EIA)
  • Beta-2-glycoprotein I antibody IVD, kit, enzyme immunoassay (EIA)
  • Histone antibody IVD, kit, enzyme immunoassay (EIA)
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