Identity
- Trade Name
- Heated Eye Pad Pro FDA UDI
- Generic Name
- Eye heat therapy pack, reusable FDA UDI
- Device Name
- Ophthalmic warmer with timer FDA UDI
- Model / Reference
- Heated Eye Pad Pro FDA UDI
- Description
- Ophthalmic warmer with timer FDA UDI
Identifiers
- Primary DI / UDI-DI
- B172PRO0 FDA UDI
- FDA Product Code
- IRT FDA UDI
- GMDN Term
- Eye heat therapy pack, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5740 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Eye heat therapy pack, reusable
Heated Eye Pad Pro by Digital Heat Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Heated Eye Pad — DIGITAL HEAT CORPORATION · Class II
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
- Digital Heat Corporation
Sources (1)
- FDA UDI d8a29862-cbb4-4e26-9258-f092830e5c42 33 fields · synced Jun 6, 2026