Identity
- Trade Name
- RITE AID FDA UDI
- Generic Name
- Aneroid manual sphygmomanometer FDA UDI
- Model / Reference
- BPAG1-20RITE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00011822589949 FDA UDI
- 510(k) Number
- K193259 FDA UDI
- FDA Product Code
- DXQ FDA UDI
- GMDN Term
- Aneroid manual sphygmomanometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1120 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Aneroid manual sphygmomanometer
Rite Aid by Microlife Usa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Aneroid manual sphygmomanometer.
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Cleared under the same submission
K193259 also covers:
- Tech-Med — Dukal LLC
- Tech-Med — Dukal LLC
- Tech-Med — Dukal LLC
- Tech-Med — Dukal LLC
- Tech-Med — Dukal LLC
- Tech-Med — Dukal LLC
- GAHAM FIELD — GF Health Products, Inc
- GRAHAM FIELD — GF Health Products, Inc
- GRAHAM FIELD — GF Health Products, Inc
- GRAHAM FIELD — GF Health Products, Inc
- Tempo — HEMASOURCE
- HealthMart — STRATEGIC SOURCING SERVICES LLC
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 |
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Manufacturer
- Manufacturer
- Microlife Usa, Inc.
Sources (1)
- FDA UDI c5a3e2f1-a27a-4e9e-a117-16f10d6a4d25 33 fields · synced May 30, 2026