LMA AIRWAY MANAGEMENT 142040

GUDID 25060112313626

LMA Unique PreCurved™ Cuff Pilot™ Size 4

TELEFLEX INCORPORATED

Laryngeal airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use Laryngeal mask airway, single-use
Primary Device ID25060112313626
NIH Device Record Keya8f95ed4-5bd9-4451-86cb-69461f8767b1
Commercial Distribution StatusIn Commercial Distribution
Brand NameLMA AIRWAY MANAGEMENT
Version Model NumberIPN900613
Catalog Number142040
Company DUNS002348191
Company NameTELEFLEX INCORPORATED
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM
Phone+1(919)544-8000
EmailCS@TELEFLEX.COM

Device Dimensions

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Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
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Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *Dark cool environment avoid direct sunlight

Device Identifiers

Device Issuing AgencyDevice ID
GS105060112313622 [Primary]
GS115060112313629 [Package]
Contains: 05060112313622
Package: Box [10 Units]
In Commercial Distribution
GS125060112313626 [Package]
Contains: 15060112313629
Package: Carton [5 Units]
In Commercial Distribution

FDA Product Code

CAEAIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-16
Device Publish Date2018-09-15

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15060112313667LMA Unique PreCurved™ Cuff Pilot™ Size 2
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25060112313589LMA Unique™ (Silicone Cuff) Cuff Pilot™ Size 4
25060112313572LMA Unique™ (Silicone Cuff) Cuff Pilot™ Size 3
15060112313568LMA Unique™ (Silicone Cuff) Cuff Pilot™ Size 2.5
25060112313558LMA Unique™ (Silicone Cuff) Cuff Pilot™ Size 2
15060112313544LMA Unique™ (Silicone Cuff) Cuff Pilot™ Size 1.5
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25060112313473LMA Unique™ (Silicone Cuff) Size 2
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25060112313459LMA Unique™ (Silicone Cuff) Size 1
25060112312933LMA Unique PreCurved™ Size 5

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