RUSCH 501003-000090

GUDID 04026704063321

Standard connector 15 mm

TELEFLEX INCORPORATED

Tube/mask breathing circuit connector, reusable

• Primary Device ID: 04026704063321
• NIH Device Record Key: 49f8a0a2-8609-4a7d-883e-dd42298778eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RUSCH
• Version Model Number: IPN044618
• Catalog Number: 501003-000090
• Company DUNS: 002348191
• Company Name: TELEFLEX INCORPORATED
• Device Count: 10
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.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
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04026704063321 [Direct Marking]
GS1	24026704063325 [Primary]
GS1	34026704063322 [Unit of Use]
GS1	44026704063329 [Package]; Contains: 24026704063325; Package: Carton [344 Units]; In Commercial Distribution

FDA Product Code

• BTR: Tube, tracheal (w/wo connector)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-01-23
• Device Publish Date: 2016-09-23

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