RUSCH RONC-14
GUDID 24026704551273
14FR Red Rubber
TELEFLEX INCORPORATED
Indwelling urethral drainage catheter| Primary Device ID | 24026704551273 |
| NIH Device Record Key | a1f06ec3-ffcf-48a9-afbd-47a21a6bcc7f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RUSCH |
| Version Model Number | IPN053693 |
| Catalog Number | RONC-14 |
| Company DUNS | 002348191 |
| Company Name | TELEFLEX 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | true |
| Labeled No Natural Rubber Latex | false |
| 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 |
Device Dimensions
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
| Width | 6.5 Inch |
| Height | 0.5 Inch |
| Length | 11 Inch |
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
| Special Storage Condition, Specify | Between 0 and 0 *false |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04026704551279 [Primary] |
| GS1 | 24026704551273 [Package] Contains: 04026704551279 Package: Box [100 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K010420
FDA Product Code
| KOD | CATHETER, UROLOGICAL |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 9 |
| Public Version Date | 2020-12-04 |
| Device Publish Date | 2016-09-16 |
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 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.