Identity
- Trade Name
- REMI FDA UDI
- Generic Name
- Electroencephalographic monitoring system FDA UDI
- Device Name
- REMI 4 Pack Disposable Sticker Accessory FDA UDI
- Model / Reference
- 20185 FDA UDI
- Description
- REMI 4 Pack Disposable Sticker Accessory FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00860011072492 FDA UDI
- FDA Product Code
- GXY FDA UDI
- GMDN Term
- Electroencephalographic monitoring system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1320 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Category: Electroencephalographic monitoring system
Remi by Epitel, Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Epitel, Inc.
Sources (1)
- FDA UDI 65d8dcf9-b575-47fa-8391-df1cf7afa6f4 34 fields · synced May 30, 2026