| Primary Device ID | 03661522100882 |
| NIH Device Record Key | b06d0c55-7d1e-4bbe-bdda-0984aa208919 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Applier, hemostatic clip |
| Version Model Number | PJT128-EB |
| Company DUNS | 265741780 |
| Company Name | PETERS SURGICAL |
| 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 | true |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 03661522100882 [Primary] |
| HBT | Applier, Hemostatic Clip |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
[03661522100882]
Dry Heat Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-01-10 |
| Device Publish Date | 2024-01-02 |