2700 NRBV CR2085

GUDID 00817136027050

2700 2W 22OD INH 35MM EXH/MP

HANS RUDOLPH, INC.

Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable Non-rebreathing valve, reusable

• Primary Device ID: 00817136027050
• NIH Device Record Key: 85c10108-4c8a-4f30-972e-fe477f001519
• Commercial Distribution Discontinuation: 2023-06-30
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 2700 NRBV
• Version Model Number: 2700
• Catalog Number: CR2085
• Company DUNS: 007131725
• Company Name: HANS RUDOLPH, INC.
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817136027050 [Primary]

FDA Product Code

• CBP: Valve, Non-Rebreathing

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: 2023-03-20
• Device Publish Date: 2023-03-10

On-Brand Devices [2700 NRBV]

• 00817136025926: 2700CB 2 WAY NRBV W/BODY SALIVA
• 00817136026176: 2700 2W NRBV W/MPORT SMC FMTR
• 00817136026213: 2700 VLV W/1.375 ID ORING MPC
• 00817136027050: 2700 2W 22OD INH 35MM EXH/MP
• 00817136027609: 2700 2W IDTPR MPORT & 22ID INH