TRUCLEARTM Calibration Insert 2.9 72203506

GUDID 00885554026061

TRUCLEAR CALIBRATION INSERT 2.9

Smith & Nephew, Inc.

Hysteroscopic irrigation/insufflation system

• Primary Device ID: 00885554026061
• NIH Device Record Key: 6b2c23d8-9034-44ae-a5ae-8bc2bd38fbf9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TRUCLEARTM Calibration Insert 2.9
• Version Model Number: 72203506
• Catalog Number: 72203506
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• 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: false
• Lot Batch: true
• 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

Customer Support Contacts

• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885554026061 [Primary]

FDA Product Code

• HIH: HYSTEROSCOPE (AND ACCESSORIES)

Sterilization

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

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

[00885554026061]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-01-31
• Device Publish Date: 2015-08-29

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• 00885556903476 - EVOS: 2025-09-08 EVOS PELVIC 5.0MM X 55MM CANNULATED SCREW PARTIALLY THREADED 32MM
• 00885556903483 - EVOS: 2025-09-08 EVOS PELVIC 5.0MM X 60MM CANNULATED SCREW PARTIALLY THREADED 32MM
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