LEWIN

GUDID 06976041612011

Shandong Lewin Medical Equipment Co., Ltd.

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Primary Device ID06976041612011
NIH Device Record Keydfce9c96-9bfe-4665-b156-2cd74b66ab9d
Commercial Distribution StatusIn Commercial Distribution
Brand NameLEWIN
Version Model NumberCreBle 1000
Company DUNS546175601
Company NameShandong Lewin Medical Equipment 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 Usefalse
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
GS106976041612011 [Primary]

FDA Product Code

GDCTable, Operating-Room, Electrical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-02-17
Device Publish Date2023-02-09

On-Brand Devices [LEWIN]

06976041611069CreLed 3300
06976041613049CreLife 6000
06976041613032CreLife 3000
06976041613025CreLife 2000
06976041613018CreLife 100
06976041612066CreBle 2100
06976041612059CreBle 1500
06976041612042CreBle 200
06976041612035CreBle 3000
06976041612028CreBle 2000
06976041612011CreBle 1000
06976041611144CreLed 150M
06976041611137CreLed 310M
06976041611120Hollow CreLed 5500M
06976041611113CreLed 3300M
06976041611106CreLed 5500M
06976041611090Hollow CreLed 5500
06976041611083Hollow CreLed 5700
06976041611076Hollow CreLed 5700/5500
06976041611052CreLed 3400
06976041611045CreLed 3400/3300
06976041611038CreLed 5500
06976041611021CreLed 5700
06976041611014CreLed 5700/5500

Trademark Results [LEWIN]

Mark Image

Registration | Serial
Company
Trademark
Application Date
LEWIN
LEWIN
85911099 4450743 Live/Registered
OptumInsight, Inc.
2013-04-22

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