Identity
- Trade Name
- Serim® PeriScreen™ Test Strips FDA UDI
- Generic Name
- Leukocyte esterase IVD, kit, rapid colorimetric, clinical FDA UDI
- Device Name
- Serim PeriScreen Test Strips indicate the presence of leukocytes (white blood cells) in peritoneal dialysate effluent. FDA UDI
- Model / Reference
- 5122 FDA UDI
- Description
- Serim PeriScreen Test Strips indicate the presence of leukocytes (white blood cells) in peritoneal dialysate effluent. FDA UDI
Identifiers
- Catalog Number
- 5122 FDA UDI
- Primary DI / UDI-DI
- M17451221 FDA UDI
- 510(k) Number
- K000578 FDA UDI
- FDA Product Code
- LJX FDA UDI
- GMDN Term
- Leukocyte esterase IVD, kit, rapid colorimetric, clinical FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.7675 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Leukocyte esterase IVD, kit, rapid colorimetric, clinical
Serim® PeriScreen™ Test Strips by Serim Research Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Serim Research Corp.
Sources (1)
- FDA UDI b2820dbd-6d26-4679-ad2d-0a8b23da23ed 37 fields · synced May 31, 2026