KD

GUDID 06970575220049

SUZHOU KD INTELLIGENT DEVICE CO., LTD

Electric-motor-driven wheelchair, occupant-controlled
Primary Device ID06970575220049
NIH Device Record Keye8dc591f-db0b-4490-86be-10d2c823b63b
Commercial Distribution StatusIn Commercial Distribution
Brand NameKD
Version Model NumberPL001-3000
Company DUNS544250984
Company NameSUZHOU KD INTELLIGENT DEVICE CO., LTD
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 Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS106970575220049 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ITIWheelchair, Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-08-21
Device Publish Date2024-08-13

On-Brand Devices [KD]

06970575220179PL001-3005
06970575220162PL001-4001
06970575220155PL001-7003
06970575220148PL001-7002
06970575220124PL001-3003
06970575220117PL001-2004
06970575220100PL001-2010
06970575220094PL001-2003
06970575220087PL001-8002
06970575220186PL001-8000
06970575220131PL001-7000
06970575220070PL001-6000
06970575220063PL001-5000
06970575220056PL001-4000
06970575220049PL001-3000
06970575220032PL001-2000
06970575220025PL001-1000
06970575220018PL001

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