Identity
- Trade Name
- Artic Flex FDA UDI
- Generic Name
- Eye mask FDA UDI
- Device Name
- Eye Gel Mask FDA UDI
- Model / Reference
- RHB1063BLU FDA UDI
- Description
- Eye Gel Mask FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00818323024463 FDA UDI
- FDA Product Code
- IME FDA UDI
- GMDN Term
- Eye mask FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5700 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Eye mask
Artic Flex by Vive Health Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Eye mask.
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- Motif BiliTouch — Wenzhou Celecare Medical lnstruments Co., Ltd. · Class I
- Bausch + Lomb — Bausch & Lomb Incorporated · Class I
- Visitec® — Beaver-Visitec International, Inc. · 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 |
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Manufacturer
- Manufacturer
- Vive Health Llc
Sources (1)
- FDA UDI cce55486-a209-4a1a-982c-32ffa5181585 33 fields · synced May 30, 2026