Cramer Decker Medical

GUDID 10816505020705

Cramer Decker Medical

Non-fixed medical gas cylinder regulator
Primary Device ID10816505020705
NIH Device Record Key9275127f-dbe9-4179-b34a-b9bce0ebfe72
Commercial Distribution StatusIn Commercial Distribution
Brand NameCramer Decker Medical
Version Model NumberAREG8704
Company DUNS041036187
Company NameCramer Decker Medical
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS100816505020708 [Primary]
GS110816505020705 [Package]
Contains: 00816505020708
Package: [20 Units]
In Commercial Distribution

FDA Product Code

CANRegulator, Pressure, Gas Cylinder

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-02-08
Device Publish Date2022-01-31

On-Brand Devices [Cramer Decker Medical]

10816505020767AREG8725-B2D
10816505020750AREG8715ME
10816505020743AREG8715
10816505020736AREG8708
10816505020712AREG8704-GREEN-PROMOLIFE
10816505020705AREG8704
10816505020699AREG5415
10816505020682AREG5408
10816505020675AREG5404-SILVER-PROMOLIFE
10816505020668AREG5404-NS-BLUE-PROMOLIFE
10816505020651AREG5404-BU-BAAD
10816505020644AREG5404

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.