Lerado

GUDID 06973134780183

LERADO ZHONGSHAN PEACEFUL COVE BUSINESS TRADING Co., Ltd.

Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable Handgrip disability-assistive walker, non-powered, foldable
Primary Device ID06973134780183
NIH Device Record Key5f7c421b-9c4a-4182-a60f-890dec28f0ef
Commercial Distribution StatusIn Commercial Distribution
Brand NameLerado
Version Model NumberRU4038
Company DUNS420676175
Company NameLERADO ZHONGSHAN PEACEFUL COVE BUSINESS TRADING Co., Ltd.
Device Count1
DM Exempttrue
Pre-market Exempttrue
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 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
GS106973134780183 [Primary]

FDA Product Code

ITJWalker, Mechanical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-04
Device Publish Date2023-09-26

On-Brand Devices [Lerado]

06973134780275PW1800
06973134780237DR4202
06973134780220RU4022
06973134780213RU4032
06973134780183RU4038
06973134780121MK1000
06973134780114MK2218
06973134780107SB4023
06973134780091SB3023
06973134780084SM3141
06973134780060SM4141
06973134780039DF4110

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.