| Primary Device ID | 00887919083061 |
| NIH Device Record Key | 7fae9815-dc7a-4503-84c7-fb715959c3c1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | STERNUM SAW BLADES |
| Version Model Number | KM-279 |
| Company DUNS | 082080136 |
| Company Name | Peter Brasseler Holdings, LLC |
| 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 | 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 | 00887919083061 [Primary] |
| GFA | BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
[00887919083061]
Radiation Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-03-28 |
| Device Publish Date | 2025-03-20 |
| 00887919084693 | KM-97 |
| 00887919084747 | KM-98 |
| 00887919083399 | KM-32 |
| 00887919083214 | KM-31 |
| 00887919083061 | KM-279 |
| 00887919130567 | ST6207-97-101N |