Identity
- Trade Name
- ARCHITECT FDA UDI
- Generic Name
- Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry FDA UDI
- Device Name
- Quantia ASO FDA UDI
- Model / Reference
- 6K38-50 FDA UDI
- Description
- Quantia ASO FDA UDI
Identifiers
- Catalog Number
- 06K3850 FDA UDI
- Primary DI / UDI-DI
- 00380740057701 FDA UDI
- FDA Product Code
- GTQ FDA UDI
- GMDN Term
- Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.3720 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry
Architect by Abbott Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry.
- Optilite Anti-Streptolysin-O Kit — The Binding Site Group · Class I
- ABX PENTRA ASO CP — Horiba Abx · Class I
- VITROS — Ortho-Clinical Diagnostics · Class I
- Tina-quant Antistreptolysin O — Roche Diagnostics Corp. · Class I
- Dimension Vista®Antistreptolysin O Flex® reagent cartridge — SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Class I
- Anti-Streptolysin O (ASO) — Randox Laboratories, Ltd. · Class I
- ANTI-STREPTOLYSIN-O 2 (ASO 2) — Randox Laboratories, Ltd. · Class I
- Antistreptolysin O AMR Fluid — The Binding Site Group · Class I
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Abbott Laboratories, Inc.
Sources (1)
- FDA UDI a7cc28ac-76b4-4d64-8c49-061b1ab559a5 36 fields · synced May 30, 2026