TRIAL CUP D68 mm

GUDID 08057968712102

HPF SRL

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Primary Device ID08057968712102
NIH Device Record Key0e4f0824-399d-40c0-aca0-7248cfd19c22
Commercial Distribution StatusIn Commercial Distribution
Brand NameTRIAL CUP D68 mm
Version Model NumberH0030156209
Company DUNS895802853
Company NameHPF SRL
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 Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108057968712102 [Primary]

FDA Product Code

HWTTemplate

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


[08057968712102]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-09-19
Device Publish Date2022-09-09

On-Brand Devices [TRIAL CUP D68 mm ]

080579687195909055.28.468
08057968712102H0030156209

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