Primary Device ID | 00810396020090 |
NIH Device Record Key | 263780bc-71b6-4cf1-841f-6f61c1f0fff9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | The Stork OTC |
Version Model Number | 1000-009 |
Company DUNS | 968804521 |
Company Name | STORK IB2C, INC., THE |
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 | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Phone | 412-200-7996 |
info@rinovum.com | |
Phone | 412-200-7996 |
info@rinovum.com |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810396020090 [Primary] |
OBB | Kit, Conception-Assist, Home Use |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-10-11 |
00810396020335 | The Stork, Merck Femibion |
00810396020311 | Stork OTC, Walgreens, S-Box |
00810396020304 | Stork OTC, General, S-Box |
00810396020199 | The Stork OTC, General |
00810396020090 | The Stork, UK |
00810396020083 | The Stork OTC, CVS |