Reliance
GUDID 00850020301348
HAAG-STREIT USA, INC.
ENT examination/treatment system| Primary Device ID | 00850020301348 |
| NIH Device Record Key | d4f82378-9fc6-47b8-b897-09866b0d6cc2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Reliance |
| Version Model Number | 610 ENT Cabinet |
| Company DUNS | 080962286 |
| Company Name | HAAG-STREIT USA, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850020301348 [Primary] |
FDA Product Code
| ETF | Unit, Examining/Treatment, Ent |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-17 |
| Device Publish Date | 2020-09-09 |
On-Brand Devices [Reliance]
Trademark Results [Reliance]
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.