| Primary Device ID | 00815067043354 |
| NIH Device Record Key | 4b1eb82f-acab-424b-82ce-878ebdeb7d87 |
| Commercial Distribution Discontinuation | 2019-05-24 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | MERIDIAN MEDICAL / LEIKA |
| Version Model Number | 3102M-L |
| Company DUNS | 800450475 |
| Company Name | Meridian Medical |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | false |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00815067043354 [Primary] |
| FNM | Mattress, Air Flotation, Alternating Pressure |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-05-24 |
| Device Publish Date | 2017-01-09 |
| 00815067043613 - MERIDIAN | 2021-01-25 SGU 84" SAFE-T-GUARD |
| 00815067043156 - MERIDIAN | 2020-03-09 SGU 48" Universal SAFE-T-GUARD |
| 00815067043224 - MERIDIAN | 2020-03-09 SGU 42" Universal SAFE-T-GUARD |
| 00815067043279 - MERIDIAN | 2020-03-09 SGU Universal SAFE-T-GUARD |
| 30815067040040 - Meridian Medical | 2019-08-20 FULL LEG INSERT LONG |
| 30815067040118 - Meridian Medical | 2019-08-20 HALF LEG INSERT |
| 30815067040231 - Meridian Medical | 2019-08-20 FULL LEG INSERT MED |
| 00815067043002 - Meridian | 2019-08-20 |