HA90AM

GUDID 00860011173670

HILL LABORATORIES CO.

Examination/treatment table, line-powered
Primary Device ID00860011173670
NIH Device Record Keyca9573a9-5bae-4ed4-99df-57575c49319d
Commercial Distribution StatusIn Commercial Distribution
Brand NameHA90AM
Version Model NumberHA90AM
Company DUNS002326585
Company NameHILL LABORATORIES CO.
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 Usetrue
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-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100860011173670 [Primary]

FDA Product Code

INQTable, Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-31
Device Publish Date2023-10-23

Devices Manufactured by HILL LABORATORIES CO.

00850058158143 - The SAVE Program2024-03-19
00850058158006 - HA90R2023-11-01
00850058158051 - HA90P2023-11-01
00850058158068 - HA90PH2023-11-01
00850058158075 - HA90PT2023-11-01
00850058158082 - HA90V2023-11-01
00850058158099 - HA90W2023-11-01
00850058158105 - HI-LO2023-11-01

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