INTERCEPTRE 7208301D

GUDID 00885556609422

DEMO HANDLE RATCHET ASSY INTERCEP

Smith & Nephew, Inc.

Surgical instrument handle, non-torque-limiting

• Primary Device ID: 00885556609422
• NIH Device Record Key: de8f74d6-7bc8-4281-a913-c31e2223124d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INTERCEPTRE
• Version Model Number: 7208301D
• Catalog Number: 7208301D
• 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)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM
• Phone: +1(800)238-7538
• Email: GUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885556609422 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K970151

FDA Product Code

• HET: LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)

Sterilization

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

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

[00885556609422]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-08-09
• Device Publish Date: 2017-08-15

On-Brand Devices [INTERCEPTRE]

• 00885556609422: DEMO HANDLE RATCHET ASSY INTERCEP
• 03596010380944: INTERCEPTRE E/S HANDLE
• 03596010380920: SCSRS HOOK INTRCPTR
• 03596010515827: CAP ROTR HDL 5MM INTRCPTR
• 03596010380937: HANDLE RATCHET ASSY INTERCEP
• 03596010380814: TRAY INSERT INTRCPTR INST.