Identity
- Trade Name
- ANA-8Pro ELISA FDA UDI
- Generic Name
- Multiple extractable nuclear antigen antibody (anti-ENA) screening IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- The ANA-8Pro ELISA is a solid phase enzyme immunoassay for the separate qualitative detection of IgG antibodies against eight cellular and nuclear antigens in human serum. The wells are separately coated with recombinant 70 kDa U1 snRNP, SS-B, SS-A 52 kDa, Scl 70, centromere protein B (CenpB), Jo-1 and highly purified native human snRNP/Sm, Sm and SS-A 60 kDa. The assay is an aid in the differential diagnosis of systemic rheumatic diseases and should be used in conjunction with other serological tests and clinical findings. FDA UDI
- Model / Reference
- 35-ANAHU-E01 FDA UDI
- Description
- The ANA-8Pro ELISA is a solid phase enzyme immunoassay for the separate qualitative detection of IgG antibodies against eight cellular and nuclear antigens in human serum. The wells are separately coated with recombinant 70 kDa U1 snRNP, SS-B, SS-A 52 kDa, Scl 70, centromere protein B (CenpB), Jo-1 and highly purified native human snRNP/Sm, Sm and SS-A 60 kDa. The assay is an aid in the differential diagnosis of systemic rheumatic diseases and should be used in conjunction with other serological tests and clinical findings. FDA UDI
Identifiers
- Catalog Number
- 35-ANAHU-E01 FDA UDI
- Primary DI / UDI-DI
- B24235ANAHUE010 FDA UDI
- 510(k) Number
- K032469 FDA UDI
- FDA Product Code
- LJM FDA UDI
- GMDN Term
- Multiple extractable nuclear antigen antibody (anti-ENA) screening IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.5100 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
ANA-8Pro ELISA by American Laboratory Products Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K032469 also covers:
- AESKULISA® ANA-8Pro — Aesku.Diagnostics GmbH & Co. KG
- AESKULISA® ANA-8Pro — Aesku.Diagnostics GmbH & Co. KG
- AESKULISA® ENA-6Pro — Aesku.Diagnostics GmbH & Co. KG
- AESKULISA® ENA-6Pro — Aesku.Diagnostics GmbH & Co. KG
- AESKULISA® Jo-1 — Aesku.Diagnostics GmbH & Co. KG
- AESKULISA® Jo-1 — Aesku.Diagnostics GmbH & Co. KG
- AESKULISA® SS-B — Aesku.Diagnostics GmbH & Co. KG
- AESKULISA® SS-B — Aesku.Diagnostics GmbH & Co. KG
- AESKULISA® Scl-70 — Aesku.Diagnostics GmbH & Co. KG
- AESKULISA® Scl-70 — Aesku.Diagnostics GmbH & Co. KG
- AESKULISA® Sm — Aesku.Diagnostics GmbH & Co. KG
- AESKULISA® Sm — Aesku.Diagnostics GmbH & Co. KG
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- American Laboratory Products Company
Sources (1)
- FDA UDI 9375578a-aa3b-49e8-bed9-d08d6b206195 38 fields · synced May 30, 2026