Acumed

GUDID B504GS500XL0

Provision

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• Primary Device ID: B504GS500XL0
• NIH Device Record Key: d55ead05-e277-4695-b38b-c38e59e1cbcc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Acumed
• Version Model Number: 500XL
• Company DUNS: 016889401
• Company Name: Provision
• Device Count: 1
• DM Exempt: true
• 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: 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B504GS500XL0 [Primary]

FDA Product Code

• KDC: Instrument, Surgical, Disposable

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: 2024-05-27
• Device Publish Date: 2024-05-17

On-Brand Devices [Acumed]

• B504OMMSDCR200: MS-DCR20
• B504OMMSDC280: MS-DC28
• B504OMAT2ML18130: AT2M-L1813
• B504OMAT2M18130: AT2M-1813
• B504OM8003870: 80-0387
• B504OM8003180: 80-0318
• B504OM8001000: 80-0100
• B504OMKM310690: 310.69
• B504OMK8009460: 80-0946
• 08100410601643: AT2M-L1813
• 08100410601629: 80-0318
• 08100410601612: 80-0100
• 08100410600882: 80-0387
• 08100410601667: MS-DCR20
• 08100410601650: MS-DC28
• 08100410601636: AT2M-1813
• B504OM101700540: 10170054
• B504OM101700530: 10170053
• B504OM101700520: 10170052
• B504OM101700510: 10170051
• 00810041060877: 80-0387
• 00810041061652: MS-DCR20
• 00810041061645: MS-DC28
• 00810041061638: AT2M-L1813
• 00810041061621: AT2M-1813
• 00810041061614: 80-0318
• 00810041061607: 80-0100
• B504OM8007720: 80-0772
• B504OM8001480: 80-0148
• B504OM8010880: 80-1088
• B504OM8006270: 80-0627
• B504OM8023790: 80-2379
• B504OM8023780: 80-2378
• B504OM8020750: 80-2075
• B504OMMSDC350: MS-DC35
• B504OM8017960: 80-1796
• B504OMAT2L25150: AT2-L2515
• B504OM8025020: 80-2502
• B504OM8020080: 80-2008
• B504OMMSDC50200: MS-DC5020
• B504OM8008680: 80-0868
• B504OM8007240: 80-0724
• B504OMBG80100: BG-8010
• B504OM8015220: 80-1522
• B504OM8025030: 80-2503
• B504OMBG8006S0: BG-8006-S
• B504OM8015920: 80-1592
• B504OMFPD200: FPD 2.0
• B504OMATF0320: ATF-032
• B504OMATF0240: ATF-024