| Primary Device ID | 00812337020381 |
| NIH Device Record Key | 01677adc-ca10-4244-ba05-073a85c79f9b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MemGuide |
| Version Model Number | 30076-02 |
| Catalog Number | 7352030 |
| Company DUNS | 131107757 |
| Company Name | DSM BIOMEDICAL, INC. |
| 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 |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Length | 30 Millimeter |
| Width | 20 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00812337020381 [Primary] |
| NPL | Barrier, Animal Source, Intraoral |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-08-09 |
| Device Publish Date | 2021-07-30 |
| 00812337020398 | Porcine Dental Membrane |
| 00812337020381 | Porcine Dental Membrane |
| 00812337020282 | Porcine Dental Membrane |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEMGUIDE 90386533 not registered Live/Pending |
ACE Surgical Supply Co., Inc. 2020-12-16 |