Bath Liner MTCBPLLG

GUDID 00841439104101

48 x 76cm

MEDTEC, INC.

Thermoplastic-moulding water bath Thermoplastic-moulding water bath Thermoplastic-moulding water bath Thermoplastic-moulding water bath Thermoplastic-moulding water bath Thermoplastic-moulding water bath Thermoplastic-moulding water bath Thermoplastic-moulding water bath Thermoplastic-moulding water bath

• Primary Device ID: 00841439104101
• NIH Device Record Key: 49dcaa69-20cb-4414-a757-35749eaffc59
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bath Liner
• Version Model Number: MTCBPLLG
• Catalog Number: MTCBPLLG
• Company DUNS: 103977526
• Company Name: MEDTEC, INC.
• Device Count: 2
• DM Exempt: true
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• 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(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com
• Phone: +1(712)737-8688
• Email: radiotherapy.complaints@civcort.com

Device Dimensions

• Length: 30 Inch
• Length: 30 Inch
• Length: 30 Inch
• Length: 30 Inch
• Length: 30 Inch
• Length: 30 Inch
• Length: 30 Inch
• Length: 30 Inch
• Length: 30 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841439104101 [Primary]
GS1	10841439104108 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K933227

FDA Product Code

• IYE: Accelerator, linear, medical

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2020-03-27
• Device Publish Date: 2017-08-02

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