Shiley
GUDID 20884521815329
Oral/Nasal Endotracheal Tube, Intermediate Cuff Non DEHP
Covidien LP
Basic endotracheal tube, single-use| Primary Device ID | 20884521815329 |
| NIH Device Record Key | cf1b0009-2ca7-44d9-b4c8-b68d5cde00a9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Shiley |
| Version Model Number | 87410 |
| Company DUNS | 058614483 |
| Company Name | Covidien LP |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com | |
| Phone | +1(508)261-8000 |
| covidien.udi@covidien.com |
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Operating and Storage Conditions
| 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 |
| 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 |
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10884521815322 [Primary] |
| GS1 | 20884521815329 [Package] Contains: 10884521815322 Package: PACK_OR_INNER_PACK [10 Units] In Commercial Distribution |
| GS1 | 30884521815326 [Package] Package: CASE [10 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K233341
FDA Product Code
| BTR | Tube, tracheal (w/wo connector) |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-07-29 |
| Device Publish Date | 2024-07-21 |
On-Brand Devices [Shiley]
| 70884522007575 | TaperGuard Oral/Nasal Tracheal Tube,Murphy Eye |
| 80884522011593 | CPAP System For Dual Lumen Tracheal Tube |
| 50884522029207 | Tracheal Tube Cuffless Reinforced |
| 40884522029194 | Tracheal Tube Cuffless Reinforced |
| 40884522029187 | Tracheal Tube Cuffless Reinforced |
| 50884522029177 | Tracheal Tube Cuffless Reinforced |
| 50884522029160 | Tracheal Tube Cuffless Reinforced |
| 40884522029156 | Tracheal Tube Cuffless Reinforced |
| 40884522029149 | Tracheal Tube Cuffless Reinforced |
| 50884522007533 | TaperGuard Oral/Nasal Tracheal Tube,Murphy Eye |
| 30884522007140 | Tracheostomy Tube Cuffed with Inner Cannula |
| 50884522007137 | Tracheostomy Tube Cuffed with Inner Cannula |
| 50884522007120 | Tracheostomy Tube Cuffed with Inner Cannula |
| 50884522007113 | Tracheostomy Tube Cuffed with Inner Cannula |
| 50884522007038 | Tracheostomy Tube Cuffed with Inner Cannula,Fenestrated |
| 50884522007021 | Tracheostomy Tube Cuffed with Inner Cannula,Fenestrated |
| 50884522006987 | Tracheostomy Tube Cuffed with Inner Cannula,Fenestrated |
| 50884522006970 | Tracheostomy Tube Cuffless with Inner Cannula |
| 50884522006963 | Tracheostomy Tube Cuffless with Inner Cannula |
| 50884522006956 | Tracheostomy Tube Cuffless with Inner Cannula |
| 40884522006942 | Tracheostomy Tube Cuffless with Inner Cannula |
| 50884522006734 | Inner Cannula XLT,Disposable |
| 50884522006727 | Inner Cannula XLT,Disposable |
| 40884522006713 | Inner Cannula XLT,Disposable |
| 30884522006501 | Nasal RAE Tracheal Tube Cuffless,Murphy Eye |
| 70884522005359 | Cap |
| 50884522005331 | Inner Cannula,Fenestrated, Disposable |
| 40884522005327 | Inner Cannula,Disposable |
| 40884522005297 | Inner Cannula,Fenestrated, Disposable |
| 50884522005287 | Inner Cannula,Disposable |
| 40884522005259 | Inner Cannula,Fenestrated, Disposable |
| 50884522005249 | Inner Cannula,Disposable |
| 50884522005218 | Inner Cannula,Fenestrated, Disposable |
| 50884522005201 | Inner Cannula,Disposable |
| 10884522004053 | Oral RAE Tracheal Tube Cuffed,Murphy Eye |
| 20884522000786 | Hi-Lo Oral/Nasal Tracheal Tube Cuffed,Intermediate, Murphy Eye |
| 30884522000165 | Hi-Lo Oral/Nasal Tracheal Tube Cuffed,Murphy Eye |
| 40884521133137 | Nasopharyngeal Airway |
| 40884521133120 | Nasopharyngeal Airway |
| 50884521133110 | Nasopharyngeal Airway |
| 50884521133103 | Nasopharyngeal Airway |
| 40884521133083 | Nasopharyngeal Airway |
| 40884521133076 | Nasopharyngeal Airway |
| 60884522007721 | Speaking Valve |
| 60884522007103 | Laryngectomy Tube |
| 60884522007097 | Laryngectomy Tube |
| 60884522007080 | Laryngectomy Tube |
| 40884522007017 | Tracheostomy Tube Cuffed with Inner Cannula,Fenestrated |
| 60884522006939 | Tracheostomy Tube Cuffless with Inner Cannula,Fenestrated |
| 60884522006915 | Tracheostomy Tube Cuffless with Inner Cannula,Fenestrated |
Trademark Results [Shiley]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 SHILEY 87453058 5667132 Live/Registered |
Covidien LP 2017-05-17 |
 SHILEY 73109823 1107132 Live/Registered |
SHILEY LABORATORIES, INC. 1976-12-16 |
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