Identity
- Trade Name
- RITEAID FDA UDI
- Generic Name
- Acupressure wristband FDA UDI
- Device Name
- RITEAID MOTION BAND FDA UDI
- Model / Reference
- 079573101988 FDA UDI
- Description
- RITEAID MOTION BAND FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00011822820134 FDA UDI
- FDA Product Code
- MVV FDA UDI
- GMDN Term
- Acupressure wristband FDA UDI
Classification
- Device Class
- U 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
Yes
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: Acupressure wristband
Riteaid by Rite Aid Corporation — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 U | Pending data |
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Manufacturer
- Manufacturer
- Rite Aid Corporation
Sources (1)
- FDA UDI 422d10a2-f8e2-4804-8d9c-20346df2039a 33 fields · synced Jun 1, 2026