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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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Sarstedt Aktiengesellschaft & Co.KG
83.3932.500
In Commercial Distribution

  • 04038917371445 ()
  • 04038917371438 ()
83.3932.500

  • Tissue culture/microbiology petri dish, single-use
No Description
Sarstedt Aktiengesellschaft & Co.KG
83.3932.300
In Commercial Distribution

  • 04038917371414 ()
  • 04038917371407 ()
83.3932.300

  • Tissue culture/microbiology petri dish, single-use
No Description
Sarstedt Aktiengesellschaft & Co.KG
83.3932.101
In Commercial Distribution

  • 04038917371384 ()
  • 04038917371377 ()
83.3932.101

  • Tissue culture/microbiology petri dish, single-use
No Description
Sarstedt Aktiengesellschaft & Co.KG
83.3932.041
In Commercial Distribution

  • 04038917371353 ()
  • 04038917371346 ()
83.3932.041

  • Tissue culture/microbiology petri dish, single-use
No Description
Sarstedt Aktiengesellschaft & Co.KG
83.3932.040
In Commercial Distribution

  • 04038917371322 ()
  • 04038917371315 ()
83.3932.040

  • Tissue culture/microbiology petri dish, single-use
No Description
Sarstedt Aktiengesellschaft & Co.KG
83.3922.005
In Commercial Distribution

  • 04038917360203 ()
  • 04038917360197 ()
83.3922.005

  • Tissue culture/microbiology petri dish, single-use
No Description
Sarstedt Aktiengesellschaft & Co.KG
83.3922.500
In Commercial Distribution

  • 04038917338585 ()
83.3922.500

  • Tissue culture/microbiology petri dish, single-use
No Description
Sarstedt Aktiengesellschaft & Co.KG
83.3922.300
In Commercial Distribution

  • 04038917338554 ()
83.3922.300

  • Tissue culture/microbiology petri dish, single-use
No Description
Sarstedt Aktiengesellschaft & Co.KG
83.3922
In Commercial Distribution

  • 04038917338523 ()
83.3922

  • Tissue culture/microbiology petri dish, single-use
For use with the Aquadex System. The Aquadex System is indicated for: Continuous ultrafiltration therapy for temporary (up to 8 hours) or extended (longer than 8 hours in patients who require hospitalization) use in adult and pediatric patients weighing 20 kilograms or more whose fluid overload is unresponsive to medical management, including diuretics. All treatments must be administered within an outpatient or inpatient clinical setting by a healthcare provider, under physician prescription, both of whom having received training in extracorporeal therapies.
Nuwellis Inc.
210104
In Commercial Distribution

  • 30853072007306 ()
  • 10853072007289 ()
210104

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