| Primary Device ID | B740TE0240 |
| NIH Device Record Key | 50a5c82b-0c78-43e2-8493-5e3483fe497d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Dr. Brown's |
| Version Model Number | TE024 |
| Company DUNS | 055872634 |
| Company Name | HANDI-CRAFT COMPANY |
| 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 | true |
| 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 |
| Phone | 1-800-778-9001 |
| info@handi-craft.com | |
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| Phone | 1-800-778-9001 |
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| Phone | 1-800-778-9001 |
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| Phone | 1-800-778-9001 |
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| Phone | 1-800-778-9001 |
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| Phone | 1-800-778-9001 |
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| info@handi-craft.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B740TE0240 [Primary] |
| KKO | Ring, Teething, Fluid-Filled |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-02-08 |
| Device Publish Date | 2022-01-31 |