Nellcor Pulse Oximeter Probe

GUDID 10861317020542

Nellcor OxiMax MAX-AL ADULT

RENU MEDICAL, INC

Pulse oximeter probe, reprocessed

• Primary Device ID: 10861317020542
• NIH Device Record Key: 7170bff9-2ed3-4e9d-851a-187c00003617
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Nellcor Pulse Oximeter Probe
• Version Model Number: RM-MAX-AL
• Company DUNS: 100439103
• Company Name: RENU MEDICAL, INC
• Device Count: 1
• 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: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00861317020545 [Primary]
GS1	10861317020542 [Package]; Contains: 00861317020545; Package: CASE [24 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K111773

FDA Product Code

• NLF: Oximeter, Reprocessed

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-08-23

On-Brand Devices [Nellcor Pulse Oximeter Probe]

• 10861317020566: Nellcor OxiMax MAX-N NEONATAL/ADULT
• 10861317020559: Nellcor OxiMax MAX-I INFANT
• 10861317020542: Nellcor OxiMax MAX-AL ADULT
• 10861317020535: Nellcor OxiMax MAX-A ADULT
• 10861317020528: Nellcor Oxisensor D-25
• 10816317020566: Nellcor OxiMax MAX-N NEONATAL/ADULT
• 10816317020559: Nellcor OxiMax MAX-I INFANT
• 10816317020542: Nellcor OxiMax MAX-AL ADULT
• 10816317020535: Nellcor OxiMax MAX-A ADULT
• 10816317020528: Nellcor Oxisensor D-25