FDA UDI In Commercial Distribution 🇺🇸 United States

Topcare

DI: 00036800493919 · Model: Early Ovulation Test · TOPCO ASSOCIATES, LLC
Product Codes
2
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Topcare
Primary DI
00036800493919
Version / Model
Early Ovulation Test
Company Name
TOPCO ASSOCIATES, LLC
Labeler DUNS
072943876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-07
Public Version
4
Public Version Date
2024-02-06
Public Version Status
Update
Public Device Record Key
11c0a409-2b0d-43c9-ba4a-f704c8797562

Device Description

A convenience kit consisting of 10 Topcare Ovulation Tests and 1 Topcare Pregnancy Test

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
CEP Radioimmunoassay, Luteinizing Hormone
LCX Kit, Test, Pregnancy, Hcg, Over The Counter

GMDN Terms

Code Name
60862 Natural conception assistance kit
33819 Total human chorionic gonadotropin IVD, kit, rapid ICT, clinical

Identifiers

Type ID
Package 10036800493916
Primary 00036800493919

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K042280 000
K981271 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
2 – 30 Degrees Celsius