Bioland E126
Bioland E126 is a Class II device made by Bioland Technology Ltd., listed in FDA GUDID since 14 Apr 2026 (UDI-DI 06939184612621), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06939184612621 | Date14 Apr 2026 | StatusListed |
Official records
- AccessGUDID record 06939184612621
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Bioland
- Generic name
- Infrared patient thermometer, skin
- Model / reference
- E126
- Primary DI / UDI-DI
- 06939184612621
- FDA product code
- FLL
- GMDN term
- Infrared patient thermometer, skin
- Device class
- Class II
- Regulation number
- 880.2910
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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