Alpha-D-Glucosidase (Gaa) Newborn Screening Test System
- US Product Code (FDA)
- PQUView Product Code Classification →
- US Risk Class (FDA)
- Class 2
- US Regulation (CFR)
- 21 CFR 862.1488View CFR Regulation →
- Medical specialty
- Clinical Chemistry
- GMP exempt
- No
- Implantable
- No
- Life-sustaining
- No
- Third party review
- Eligible
For quantitative measurement of the activity of alpha-D-glucosidase (GAA) from newborn dried blood spot specimens.
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Alpha-D-Glucosidase (Gaa) Newborn Screening Test System is a medical device type in the Clinical Chemistry specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.
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