Integra

GUDID B504GS1032200

Provision

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• Primary Device ID: B504GS1032200
• NIH Device Record Key: 13b5cd70-34c3-4636-9ce2-17c3ce9248b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Integra
• Version Model Number: 103-220
• 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	B504GS1032200 [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 [Integra]

• B504CT0800030: 08-0003
• B5040800030: 08-0003
• 08100410609113: 08-0003
• 00810041069108: 08-0003
• B504OM6007090: 60-0709
• B504OMSAW6949T0: SAW6949T
• B504OMSAW6948T0: SAW6948T
• B504OMSAW6945T0: SAW6945T
• B504OMLJV528T0: LJV528T
• B504OMLJV527T0: LJV527T
• B504OMLJV526T0: LJV526T
• B504OMLJV525T0: LJV525T
• B504OMSAW6951T0: SAW6951T
• B504OM2502620: 250-262
• B504OM2502610: 250-261
• B504OMPAN101000340: PAN-1010-0034
• B504OM35392520: 3539252
• B504OM33340: 33-34
• B504OMLJU097T0: LJU097T
• B504OMSAW6947T0: SAW6947T
• B504OM25026500: 250-2650
• B504GS4601070: 460-107
• B504GS1101800: 110-180
• B504GS1005430: 100-543
• B504GS1991050: 199-105
• B504GS37244030: 3724403
• B504GS1091190: 109-119
• B504GS1072200: 107-220
• B504GS2041500: 204-150
• B504GS1061310: 106-131
• B504OM1302340: 130-234
• B504GSMH61200: MH6-120
• B504GS2504100: 250-410
• B504GS2503980: 250-398
• B504GS1013000: 101-300
• B504CT0961000: 09-6100
• B504GS2853800: 285-380
• B504GS1101180: 110-118
• B504GS1032200: 103-220