Primary Device ID | 40761236900578 |
NIH Device Record Key | 56b2b298-a5d6-4360-8a2a-9d6d7e942b2c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ID Pleasure |
Version Model Number | ID Pleasure 2.2 fl oz Disc Cap Bottle |
Company DUNS | 879057065 |
Company Name | WESTRIDGE LABORATORIES INCORPORATED |
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 | false |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00761236900570 [Primary] |
GS1 | 40761236900578 [Package] Contains: 00761236900570 Package: Case [24 Units] In Commercial Distribution |
NUC | Lubricant, Personal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-08-09 |
Device Publish Date | 2018-03-06 |
20761236900734 | ID Pleasure 17 fl oz Pump |
30761236900595 | ID Pleasure 8.5 fl oz Disc Cap Bottle |
30761236900588 | ID Pleasure 4.4 fl oz Disc Cap Bottle |
40761236900578 | ID Pleasure 2.2 fl oz Disc Cap Bottle |
40761236900561 | ID Pleasure 1 fl oz Pocket Bottle |
40761236900042 | ID Pleasure 4.2 oz Retail Box (EN) |
00761236110009 | ID Pleasure 12 ml Tube |
00761236109973 | ID Pleasure 10 ml Pillow |
30761236104047 | ID Pleasure 4.1 fl oz Travel Tube |
40761236104020 | ID Pleasure 2 fl oz Travel Tube |
20761236102169 | ID Pleasure 17 oz Pump |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ID PLEASURE 78202744 2846793 Live/Registered |
Westridge Laboratories, Inc. 2003-01-13 |