Identity
- Trade Name
- Dreambaby FDA UDI
- Generic Name
- Intermittent electronic patient thermometer FDA UDI
- Device Name
- The digital thermometers are intended to measure the human body temperature in regular mode orally, rectally or under the arm, And the devices are reusable for clinical or home use on people ofall ages, including children under 8 years old with adult supervision. FDA UDI
- Model / Reference
- DMT-4726 FDA UDI
- Description
- The digital thermometers are intended to measure the human body temperature in regular mode orally, rectally or under the arm, And the devices are reusable for clinical or home use on people ofall ages, including children under 8 years old with adult supervision. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06970392210988 FDA UDI
- FDA Product Code
- FLL FDA UDI
- GMDN Term
- Intermittent electronic patient thermometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2910 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dreambaby by Joytech Healthcare Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Joytech Healthcare Co., Ltd
Sources (1)
- FDA UDI e70ed534-6c85-4163-a2f7-d255e65c32b8 34 fields · synced May 30, 2026