| Primary Device ID | 30662956935556 |
| NIH Device Record Key | ef76ea81-e7ee-4e24-850b-4229fef3d56d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Bodyguard |
| Version Model Number | 815 BK S |
| Company DUNS | 042653634 |
| Company Name | Fastenal Company |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | true |
| 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 | 00662956390316 [Primary] |
| GS1 | 30662956935556 [Package] Contains: 00662956390316 Package: BX [100 Units] In Commercial Distribution |
| GS1 | 50662956935550 [Package] Package: CASE [10 Units] In Commercial Distribution |
| LZA | Polymer Patient Examination Glove |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-01 |
| Device Publish Date | 2023-05-24 |
| 03066295694406 | 816EI |
| 30662956935570 | 815 BK XL |
| 30662956935556 | 815 BK S |
| 00662956390170 | 815 BK L |
| 30662956935563 | 815 BK M |
| 00662956211550 | 816EI VP |
| 30662956500471 | XL SERIES 814E 4 MIL BLUE NITRILE EXAM GRADE POWDER-FREE BODY GUARD[REG] DISPOSABLE GLOVE |
| 30662956500464 | LARGE SERIES 814E 4 MIL BLUE NITRILE EXAM GRADE POWDER-FREE BODY GUARD[REG] DISPOSABLE GLOVE |
| 30662956500457 | MEDIUM SERIES 814E 4 MIL BLUE NITRILE EXAM GRADE POWDER-FREE BODY GUARD[REG] DISPOSABLE GLOVE |
| 30662956500433 | SMALL SERIES 814E 4 MIL BLUE NITRILE EXAM GRADE POWDER-FREE BODY GUARD[REG] DISPOSABLE GLOVE |