FDA UDI
In Commercial Distribution
🇺🇸 United States
Luteinizing Hormone (LH) Ovulation test
DI: 06952062712671
·
Model: Midstream,1pc/Box
·
ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
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Basic Information
- Brand Name
- Luteinizing Hormone (LH) Ovulation test
- Primary DI
- 06952062712671
- Version / Model
- Midstream,1pc/Box
- Company Name
- ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD
- Labeler DUNS
- 546403492
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2026-03-20
- Public Version
- 1
- Public Version Date
- 2026-03-30
- Public Version Status
- New
- Public Device Record Key
- 6609053a-8b7d-43d3-9b39-8ea25bd05081
Device Description
LH Ovulation Test (Colloidal Gold) is a rapid chromatographic immunoassay for the qualitative detection of Luteinising Hormone (LH) in female urine to predict when there is a LH surge, and in turn, when you are likely to ovulate. This test is designed for over-the-counter use.
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- No
- Over the Counter (OTC)
- No
- Kit
- No
- 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
- Yes
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- Yes
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- No
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| NGE | Test, Luteinizing Hormone (Lh), Over The Counter | Clinical Chemistry | 862.1485 | 1 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 54255 | Luteinizing hormone (LH) IVD, kit, rapid ICT, clinical | A collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of luteinizing hormone (LH) in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. This is a rapid test used in the laboratory or in point-of-care analyses. It is not intended to be used for self-testing. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 06952062712671 | GS1 |