Primary Device ID | 00696588003627 |
NIH Device Record Key | a8d9f2aa-829d-4283-ad92-58f1cbc3ebb0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Phase 4 Gel® |
Version Model Number | 509-P4-NSP |
Catalog Number | 509-P4-NSP |
Company DUNS | 147363154 |
Company Name | Innovative Medical Products, Inc |
Device Count | 1 |
DM Exempt | true |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00696588003627 [Primary] |
FMP | Protector, Skin Pressure |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-10 |
Device Publish Date | 2022-08-02 |
00696588005621 | Sample Phase 4 Gel® Splint - Non Sterile (1 each) |
00696588003627 | Phase 4 Gel® Splint - Non Sterile (10/case) |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PHASE 4 GEL 76714911 4535142 Live/Registered |
Innovative Medical Products Inc. 2013-09-06 |
![]() PHASE 4 GEL 76697938 not registered Dead/Abandoned |
Innovative Medical Products Inc. 2009-06-17 |