PH 08 Probe Holder

GUDID 07332834000691

PH 08 Probe Holder

Perimed AB

Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter Laser Doppler blood flowmeter

• Primary Device ID: 07332834000691
• NIH Device Record Key: 9f7742f7-743f-48f9-8dcf-d03b4370c4d8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PH 08 Probe Holder
• Version Model Number: PH 08
• Company DUNS: 354765570
• Company Name: Perimed AB
• Device Count: 10
• 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: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07332834000684 [Unit of Use]
GS1	07332834000691 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K974285

FDA Product Code

• DPW: Flowmeter, Blood, Cardiovascular

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-01-11
• Device Publish Date: 2018-12-11

Devices Manufactured by Perimed AB

• 07332834000790 - PF 6840-1 TC Remote Panel 1 Channel: 2023-02-09 PF 6840-1 TC Remote Panel 1 Channel
• 07332834000806 - PF 6840-2 TC Remote Panel 2 Channels: 2023-02-09 PF 6840-2 TC Remote Panel 2 Channels
• 07332834000820 - PF 6840-4 TC Remote Panel 4 Channels: 2023-02-09 PF 6840-4 TC Remote Panel 4 Channels
• 07332834000066 - PeriFlux 6000: 2021-10-28 PeriFlux 6000
• 07332834000608 - PH 07-5 Small Tape-Fixated Probe Holder: 2021-06-02 PH 07-5 Small Tape-Fixated Probe Holder (5 pcs)
• 07332834000387 - MT B500-0L120 Straight Microtip: 2020-04-23 MT B500-0L120 Straight Microtip
• 07332834000394 - MT B500-0L240 Straight Microtip: 2020-04-23 MT B500-0L240 Straight Microtip
• 07332834000288 - TC 550 Fixation Ring for tcpO2/CO2 (50 pcs) and TC 560 Contact Liquid: 2019-12-13 Convenience kit including: TC 550 Fixation Ring for tcpO2/CO2 (50 pcs) TC 560 Contact Liquid (20 ml)