TRIAL CUP D56 mm

GUDID 08057968712041

HPF SRL

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Primary Device ID	08057968712041
NIH Device Record Key	7c032f2e-31dd-46e8-8197-5ff6470b4bbe
Commercial Distribution Status	In Commercial Distribution
Brand Name	TRIAL CUP D56 mm
Version Model Number	H0030153809
Company DUNS	895802853
Company Name	HPF SRL
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	08057968712041 [Primary]

FDA Product Code

HWT

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