Senolo

GUDID 26952534451026

JIANGSU SENOLO MEDICAL TECHNOLOGY CO., LTD.

Cast construction material
Primary Device ID26952534451026
NIH Device Record Keyfa0e3a6e-dbc3-4cf5-9860-d3b7dab3b432
Commercial Distribution StatusIn Commercial Distribution
Brand NameSenolo
Version Model NumberXE23
Company DUNS421315790
Company NameJIANGSU SENOLO MEDICAL TECHNOLOGY CO., LTD.
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 Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS126952534451026 [Primary]

FDA Product Code

ITGBandage, Cast

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-04-14
Device Publish Date2023-04-06

On-Brand Devices [Senolo]

26952534451040XE43
26952534451033XE33
26952534451026XE23
26952534441089XP8
26952534441065XP6
26952534441041XP4
26952534441034XP3
26952534441027XP2
269525344310355l
269525344310281l
26952534431011250ml
16952534421169XB546
16952534421152XB530
16952534421145XB430
16952534421138XB416
16952534421121XB336
16952534421114XB312
16952534421060XB6
16952534421053XB5
16952534421046XB4
16952534421039XB3
16952534421022XB2
16952534411160XD6
16952534411153XD5
16952534411146XD4
16952534411139XD3
16952534411122XD2

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