EM

GUDID 00026072022016

REG,O2,870,25LPM,1CK,1CPLR

ALLIED HEALTHCARE PRODUCTS, INC.

Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator Non-fixed medical gas cylinder regulator

• Primary Device ID: 00026072022016
• NIH Device Record Key: 4b6969ab-f3fb-4363-8136-952b6d126340
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EM
• Version Model Number: L370-220BC58-R
• Company DUNS: 099674145
• Company Name: ALLIED HEALTHCARE PRODUCTS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00026072022016 [Primary]

FDA Product Code

• CAN: Regulator, Pressure, Gas Cylinder

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-27
• Device Publish Date: 2023-12-19

On-Brand Devices [EM]

• 00026072026519: KIT,PKG/6,DISS CHECK VALVE
• 00026072025420: REG,O2,CGA870,0-25LPM,2CK
• 00026072024577: REG O2 870 0-25 DISS/OHMEDA CK
• 00026072024225: LSP RHINO O2 REG 870 2CHECKS
• 00026072024034: REG O2 PRESET 540 2 DISS CKS
• 00026072023808: REG,O2,CGA870,25 LPM,0CKS
• 00026072022290: REG,O2,477,25LPM,2CKS,DAN
• 00026072022115: REG,O2,CGA540,FIXED FLOW,
• 00026072022092: REG O2 870 0-25 BARB
• 00026072022085: REG O2 870 0-25 BARB
• 00026072022078: REG O2 870 0-25 BARB
• 00026072022061: REG O2 870 0-25 BARB
• 00026072022054: REG O2 870 0-25 BARB 2 CHKS
• 00026072022047: REG,O2,870,25LPM,2-HANSHIN CPL
• 00026072022030: REG O2 870 0-25 2 CHKS
• 00026072022023: REG O2 870 0-25 BARB 2 CHKS
• 00026072022016: REG,O2,870,25LPM,1CK,1CPLR
• 00026072022009: REG O2 870 0-25 BARB 2 CHECKS
• 00026072021996: REG O2 870 0-25 BARB 2 CHECKS
• 00026072021989: REG,O2,540 0-25 BARB 2CKS
• 00026072021972: REG O2 540 0-25 BARB 2 CHECKS.
• 00026072021965: REG O2 870 0-15 BARB
• 00026072021958: REG O2 870 0-25 BARB
• 00026072021941: REG O2 870 0-15 BARB 2 CHECKS
• 00026072021934: REG,O2,870,0-25 BARB
• 00026072021927: REG O2 870 0-25 BARB 2 CHECKS