bili-hut™

GUDID 00810101280023

LITTLE SPARROWS TECHNOLOGIES LLC

Overhead infant phototherapy unit
Primary Device ID00810101280023
NIH Device Record Keyd54a5ee7-f6c8-4637-b9d8-db004f5a516f
Commercial Distribution StatusIn Commercial Distribution
Brand Namebili-hut™
Version Model Number0130A
Company DUNS078764736
Company NameLITTLE SPARROWS TECHNOLOGIES LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100810101280023 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LBIUnit, Neonatal Phototherapy

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-03-18
Device Publish Date2022-03-10

On-Brand Devices [bili-hut™]

00850019925043Neonatal Jaundice Phototherapy Device
008500199250810130A
008500199250980130A
00850019925074130A
008500199258760130A
008500199258690130A
008500199257530130A
008500199257460130A
008500199257220130A
008500199257150130A
008500199255550130A
008500199255480130A
008500199255240130A
008500199255170130A
008500199255000130A
008500199254940130A
008500199254870130A
008500199254630130A
008500199254490130A
008500199254320130A
008500199254250130A
008500199254180130A
008500199254010130A
008500199253950130A
008500199253880130A
008500199253710130A
008500199253640130A
008500199253570130A
008500199250360130A
008101012804050130A
008101012800540130A
008101012800470130A
008101012800230130A
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