HA90D

GUDID 00850058158013

HILL LABORATORIES CO.

Examination/treatment table, line-powered
Primary Device ID00850058158013
NIH Device Record Key16d310a1-d394-450b-a72d-40ae44b10c2a
Commercial Distribution StatusIn Commercial Distribution
Brand NameHA90D
Version Model NumberHA90D
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
GS100850058158013 [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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