L’DISQ®

GUDID 08800015900003

U&I CORPORATION

Electrosurgical return electrode, single-use, sterile
Primary Device ID08800015900003
NIH Device Record Keyc203a876-da54-4ba2-8edb-6e0471fe5fa4
Commercial Distribution StatusIn Commercial Distribution
Brand NameL’DISQ®
Version Model NumberPD02
Company DUNS688811082
Company NameU&I CORPORATION
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place.

Device Identifiers

Device Issuing AgencyDevice ID
GS108800015900003 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-06-17
Device Publish Date2016-09-24

On-Brand Devices [L’DISQ®]

08800015911856PD07
08800015911849PD05
08800015911832PD04
08800015911825PC02
08800015911818PC01
08800015900027PD03
08800015900010PD01
08800015900003PD02

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