FDA UDI
In Commercial Distribution
🇺🇸 United States
Seracult Triple Slide Fecal Occult Blood Test
DI: 70818087013016
·
Model: 37200400
·
PROPPER MANUFACTURING COMPANY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
34
Basic Information
- Brand Name
- Seracult Triple Slide Fecal Occult Blood Test
- Primary DI
- 70818087013016
- Version / Model
- 37200400
- Company Name
- PROPPER MANUFACTURING COMPANY, INC.
- Labeler DUNS
- 001483130
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 34
- Record Status
- Published
- Publish Date
- 2019-03-07
- Public Version
- 2
- Public Version Date
- 2020-12-21
- Public Version Status
- Update
- Public Device Record Key
- 4818fd8f-53dc-4183-96a4-cdfa56bee339
Device Description
Seracult Triple Slide Fecal Occult Blood Test
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
- 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 | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| KHE | Reagent, Occult Blood | Hematology | 864.6550 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 54533 | Faecal occult blood IVD, reagent | A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative screening of stool (faeces) for occult blood (haemoglobin). | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 70818087013016 | GS1 | ||||
| Unit of Use | 10818087013014 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K834297 | 000 |