HA90M

GUDID 00850058158044

HILL LABORATORIES CO.

Examination/treatment table, line-powered
Primary Device ID00850058158044
NIH Device Record Keyd40991f2-0aec-486d-857e-08dbe84cc392
Commercial Distribution StatusIn Commercial Distribution
Brand NameHA90M
Version Model NumberHA90M
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
GS100850058158044 [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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