RUSCH 120101-000080
GUDID 44026704010415
Tracheostomy tube set, short, phonation
TELEFLEX INCORPORATED
Basic tracheostomy tube, reusable| Primary Device ID | 44026704010415 |
| NIH Device Record Key | 9dde7003-76b1-4913-aa67-cc1cb3c7303e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RUSCH |
| Version Model Number | IPN041803 |
| Catalog Number | 120101-000080 |
| Company DUNS | 002348191 |
| Company Name | TELEFLEX INCORPORATED |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | 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(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM | |
| Phone | +1(919)544-8000 |
| CS@TELEFLEX.COM |
Device Dimensions
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
| Device Size Text, specify | 0 |
| Outer Diameter | 11.4 Millimeter |
| Lumen/Inner Diameter | 8 Millimeter |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04026704010417 [Primary] |
| GS1 | 24026704010411 [Package] Contains: 04026704010417 Package: Box [2 Units] In Commercial Distribution |
| GS1 | 44026704010415 [Package] Contains: 24026704010411 Package: Carton [28 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K964056
FDA Product Code
| JOH | Tube tracheostomy and tube cuff |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-06-03 |
| Device Publish Date | 2015-10-16 |
On-Brand Devices [RUSCH]
| 24026704550191 | 1" Foam Straps |
| 24026704549843 | One Piece Medium Catheter w/o Tape |
| 24026704549836 | One Piece Regular Catheter w/o Tape |
| 44026704546723 | PVC NASOPHARYNGEAL AIRWAY KIT, STERILE |
| 44026704546716 | PVC NASOPHARYNGEAL AIRWAY KIT, STERILE |
| 44026704546709 | Ultra Robertazzi Nasopharyngeal Airway Kit, Sterile |
| 44026704546693 | Ultra Robertazzi Nasopharyngeal Airway Kit, Sterile |
| 44026704094088 | PERCUQUICK TRACHEOSTOMY SET, STERILE |
| 44026704094071 | PERCUQUICK TRACHEOSTOMY SET, STERILE |
| 44026704094064 | PERCUQUICK TRACHEOSTOMY SET, STERILE |
| 44026704067624 | Silkospray |
| 44026704066122 | Adhesive patch, big |
| 04026704063390 | Standard connector 15 mm |
| 04026704063369 | Standard connector 15 mm |
| 04026704063352 | Standard connector 15 mm |
| 04026704063345 | Standard connector 15 mm |
| 04026704063338 | Standard connector 15 mm |
| 04026704063321 | Standard connector 15 mm |
| 04026704063314 | Standard connector 15 mm |
| 04026704063307 | Standard connector 15 mm |
| 04026704063291 | Standard connector 15 mm |
| 04026704063284 | Standard connector 15 mm |
| 04026704063277 | Standard connector 15 mm |
| 04026704063260 | Standard connector 15 mm |
| 04026704063253 | Standard connector 15 mm |
| 04026704063246 | Standard connector 15 mm |
| 34026704063230 | Standard connector 15 mm |
| 34026704063223 | Standard connector 15 mm |
| 34026704063216 | Standard connector 15 mm |
| 34026704063209 | Standard connector 15 mm |
| 34026704063193 | Standard connector 15 mm |
| 34026704063186 | Standard connector 15 mm |
| 34026704063179 | Standard connector 15 mm |
| 04026704058464 | Rectal tube, 50 cm, open tip, 1 eye |
| 04026704058457 | Rectal tube, 50 cm, open tip, 1 eye |
| 04026704058440 | Rectal tube, 50 cm, open tip, 1 eye |
| 04026704058433 | Rectal tube, 50 cm, open tip, 1 eye |
| 04026704058426 | Rectal tube, 50 cm, open tip, 1 eye |
| 04026704058419 | Rectal tube, 50 cm, open tip, 1 eye |
| 44026704058400 | Rectal tube, 50 cm, open tip, 1 eye |
| 44026704058394 | Rectal tube, 50 cm, open tip, 1 eye |
| 44026704058387 | Rectal tube, 50 cm, open tip, 1 eye |
| 44026704058370 | Rectal tube, 50 cm, open tip, 1 eye |
| 44026704058363 | Rectal tube, 50 cm, open tip, 1 eye |
| 44026704058356 | Rectal tube, 50 cm, open tip, 1 eye |
| 44026704058349 | Rectal tube, 50 cm, open tip, 1 eye |
| 44026704017834 | Face mask for anesthesia, pediatric |
| 44026704017827 | Face mask for anesthesia, pediatric |
| 44026704017810 | Face mask for anesthesia, pediatric |
| 44026704017803 | Face mask for anesthesia, pediatric |
Trademark Results [RUSCH]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 RUSCH 71671275 0609663 Dead/Expired |
WILLY RUSCH K. G. 1954-08-06 |
 RUSCH 71671274 0609662 Live/Registered |
WILLY RUSCH K.G. 1954-08-06 |
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