XIA ANTERIOR 48047011L

GUDID 07613327276572

BENDING IRON, LEFT

Stryker Corporation

Manual orthopaedic bender, reusable

• Primary Device ID: 07613327276572
• NIH Device Record Key: 24af327a-c86b-47f7-9e17-db0978251da3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: XIA ANTERIOR
• Version Model Number: 48047011L
• Catalog Number: 48047011L
• Company DUNS: 149183167
• Company Name: Stryker Corporation
• Device Count: 1
• DM Exempt: false
• 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: 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	07613327276572 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[07613327276572]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2019-11-21
• Device Publish Date: 2018-09-24

On-Brand Devices [XIA ANTERIOR]

• 07613327276572: BENDING IRON, LEFT
• 07613327276503: BENDING IRON, RIGHT
• 07613327263299: INSERTER TUBE
• 07613327263107: SCREWDRIVER
• 07613327263091: CROSS CONNECTOR HOLDER
• 07613327263084: CALIPER
• 07613327263077: PARALLEL COMPRESSOR
• 07613327263060: DUAL STAPLE IMPACTOR
• 07613327263046: ANGLED AWL
• 07613327263039: PARALLEL DISTRACTER
• 07613327119886: TITANIUM IMPLANT CONTAINER LID
• 07613327119862: SCREW RACK
• 07613327118919: ANTERIOR LP INSTRUMENT CONTAINER
• 07613327118896: TITANIUM IMPLANT CONTAINER