Rescue

GUDID 26948318968620

Anrei Medical(HZ) Co.,Ltd.

Flexible endoscopic grasping forceps, single-use

• Primary Device ID: 26948318968620
• NIH Device Record Key: d833428a-51de-43ca-a4b4-79b92e2bddce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rescue
• Version Model Number: M00527551
• Company DUNS: 529128653
• Company Name: Anrei Medical(HZ) Co.,Ltd.
• Device Count: 1
• 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: 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816849017310 [Previous]
GS1	26948318968620 [Primary]

FDA Product Code

• OCZ: Endoscopic Grasping/Cutting Instrument, Non-Powered

Sterilization

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

[26948318968620]

Ethylene Oxide

[26948318968620]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-03-25
• Device Publish Date: 2019-02-28

On-Brand Devices [Rescue]

• 26948318968644: M00527751
• 26948318968637: M00527651
• 26948318968620: M00527551
• 26948318968613: M00527451
• 26948318968606: M00538351
• 16948318968807: M00527550
• 16948318903983: M00538350
• 16948318903938: M00527750
• 16948318903907: M00527650
• 16948318903822: M00527450