| Primary Device ID | 00896128002657 |
| NIH Device Record Key | fe5b0e10-842f-46f4-84a3-ed6a6142d049 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | buddy,230V SYSTEM |
| Version Model Number | 905-00001A-F-SE |
| Company DUNS | 078330362 |
| Company Name | BELMONT INSTRUMENT CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00896128002657 [Primary] |
| BSB | Warmer, Blood, Non-Electromagnetic Radiation |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2022-03-22 |
| Device Publish Date | 2016-09-23 |
| 00896128002749 | buddy, 230V SYSTEM,ENGLISH, SWITZERLAND CORD |
| 00896128002732 | buddy, 230V SYSTEM, ITALIAN, SWITZERLAND CORD |
| 00896128002725 | buddy, 230V SYSTEM,FRENCH, SWITZERLAND CORD |
| 00896128002718 | buddy, 230V SYSTEM,GERMAN, SWITZERLAND CORD |
| 00896128002701 | buddy, 230V SYSTEM, ENGLISH, UK CORD |
| 00896128002695 | buddy, 230V SYSTEM, DUTCH, STANDARD EUROPEAN CORD |
| 00896128002688 | buddy, 230V SYSTEM, ITALIAN, STANDARD EUROPEAN CORD |
| 00896128002671 | buddy, 230V SYSTEM, ENGLISH, ISRAEL CORD |
| 00896128002664 | buddy, 230V SYSTEM, GERMAN STANDARD EUROPEAN CORD |
| 00896128002121 | buddy, 230V SYSTEM, ENGLISH STANDARD EUROPEAN CORD |
| 00896128002657 | buddy, 230V SYSTEM, FRENCH STANDARD EUROPEAN CORD |