| Primary Device ID | 36939029815485 |
| NIH Device Record Key | 056c09a9-78a3-4ef5-b02e-f77979a4685d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HEBU |
| Version Model Number | HF9831-24 |
| Company DUNS | 527812392 |
| Company Name | Modern Medical Equipment MFG. Ltd. |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 | 06939029815484 [Primary] |
| GS1 | 16939029815481 [Package] Contains: 06939029815484 Package: White Box [10 Units] In Commercial Distribution |
| GS1 | 26939029815488 [Package] Contains: 16939029815481 Package: Inner Box [10 Units] In Commercial Distribution |
| GS1 | 36939029815485 [Package] Contains: 26939029815488 Package: Carton Box [10 Units] In Commercial Distribution |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2017-12-12 |
| 36939029816222 | Open-surgery electrosurgical electrode, monopolar, single-use |
| 36939029816130 | HF9834-24 |
| 36939029815485 | Open-surgery electrosurgical electrode, monopolar, single-use |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() HEBU 78011639 not registered Dead/Abandoned |
Lebow, Jan Zahler 2000-06-07 |
![]() HEBU 74135904 1729175 Dead/Cancelled |
HEINZ BUCHAL AUTOMATTENFABRIK 1991-02-04 |