FDA.reportPublic FDA data

Ventlab

Primary DI
20889483094294
Brand
Ventlab
Company
VENTLAB, LLC
Model
cprmc02
Device description
CO2 Indicator
Published
2016-10-01
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
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
K093525000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K093525000ACE/STATCHECK II CO2 INDICATOR, ACE/STATCHECK II CO2 INDICATOR ARM ASSEMBY ADULT STATCHECK RESUSCITATOR WITH ACE/STATCHEVentlab Corp.2009-12-10CCK

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
20889483094294PackageGS110In Commercial Distribution
10889483094297PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
2088948309429420889483094294
1088948309429710889483094297

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.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00General Warehouse. Do not get wet.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
800-433-2797info@sun-med.com

Regulatory Flags#

DUNS number
038305402
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10889483227046VentlabR500P21R500P212023-07-18
10889483227022VentlabR500P30R500P302023-07-17
10889483228364VentlabR500P31R500P312023-07-17
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

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