FDA.reportPublic FDA data

Ventlab

Primary DI
10889483228364
Brand
Ventlab
Company
VENTLAB, LLC
Model
R500P31
Catalog number
R500P31
Device description
MaxCap - Pediatric
Published
2023-07-17
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
CCKANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-PhaseAnesthesiology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K133540000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K133540000FLOCAPMaxtec, Inc.2014-03-28CCK

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10889483228364PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
1088948322836410889483228364

GMDN Terms#

Term, Definition table
TermDefinition
Exhaled-gas oesophageal intubation detector, adultA device designed to verify proper endotracheal (ET) tube placement by detecting/assessing escaping levels of exhaled carbon dioxide (CO2) during airway management disclosing potential incorrect intubation. It is used during adult intubation and is attached directly between the ET tube and the breathing device. It typically functions through colorimetric CO2 detection using an indicator paper that changes colour. A colour chart (e.g., attached to the device) permits interpretation into approximate CO2 concentration. It is used in healthcare facilities or in the field to evaluate oesophageal intubation, which if performed incorrectly, prevents patient ventilation. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)433-2797info@sun-med.com

Regulatory Flags#

DUNS number
038305402
Device count
1
DM exempt
true
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10889483227046VentlabR500P21R500P212023-07-18
10889483227022VentlabR500P30R500P302023-07-17
10889483228371VentlabR500P32R500P322023-07-17
10889483100745VentlabHS4251-D22016-12-22
10889483096925VentlabVR2700-20VR2700-202023-06-02
10889483098585VentlabVR2400-40VR2400-402023-06-02
10889483099094VentlabVR4700-20VR4700-202023-06-02
10889483104132VentlabVR2400-100VR2400-1002023-06-02
10889483107287VentlabVR1100-40VR1100-402023-06-02
10889483111529VentlabVR5700-20VR5700-202023-06-02
10889483112175VentlabVR2100-40VR2100-402023-06-02
10889483112298VentlabVR3700-20VR3700-202023-06-02
10889483160831VentlabVR1900-20VR1900-202023-06-02
10889483160855VentlabVR2900-20VR2900-202023-06-02
10889483160879VentlabVR3900-20VR3900-202023-06-02
10889483160930VentlabVR5900-20VR5900-202023-06-02
10889483164273VentlabVR4500-20VR4500-202023-06-02
10889483164297VentlabVR5500-20VR5500-202023-06-02
10889483164334VentlabVR7500-20VR7500-202023-06-02
10889483066782Ventlab2301F2301F2023-03-21

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Primary DI, Brand, Company table
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