OvuQuick Ovulation Predictor Test

Primary DI
10805360016015
Brand
OvuQuick Ovulation Predictor Test
Company
VITROLIFE INC.
Model
15100
Published
2016-09-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
CEPRadioimmunoassay, Luteinizing Hormone

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
CEPRadioimmunoassay, Luteinizing HormoneClinical Chemistry1

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K871726000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K871726000OVUQUICK SELF-TEST (OVUQUICK; RAMP LH ASSAY)Monoclonal Antibodies, Inc.1987-07-27CEP

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10805360016015PrimaryGS10
00805360016018Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1080536001601510805360016015
00805360016018008053600160188053600160180805360016018

GMDN Terms#

Term, Definition table
TermDefinition
Natural conception assistance kitA collection of devices intended to improve the likelihood of natural conception by monitoring ovulation and supplementing essential vitamins. The kit may contain in vitro diagnostic medical devices (IVDs) such as immunochromatographic tests for ovulation and pregnancy detection, a digital thermometer, vitamin supplements for the male and the female, and instructions for use.

Regulatory Flags#

DUNS number
051915038
Device count
6
Lot or batch
true
Expiration date on label
true

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10805360014165Handling Pipette155352021-09-03
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10805360014189Handling Pipette155372021-09-03
10805360014196Handling Pipette155382021-09-03

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