03900011

GUDID 07611819790988

SMALL SCREW REMOVAL FORCEPS

SYNTHES (U.S.A.) LP

Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps

• Primary Device ID: 07611819790988
• NIH Device Record Key: 240bf45b-0908-424b-bc0a-96fa1cbddf32
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 03.900.011
• Catalog Number: 03900011
• Company DUNS: 832637081
• Company Name: SYNTHES (U.S.A.) LP
• 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: 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)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07611819790988 [Direct Marking]
GS1	10886982080653 [Primary]
HIBCC	H679039000110 [Secondary]

FDA Product Code

• HTD: FORCEPS

Sterilization

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

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

[07611819790988]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-10-13
• Device Publish Date: 2018-07-18

Devices Manufactured by SYNTHES (U.S.A.) LP

• 10886982305909 - NA: 2021-10-25 3.5MM DRILL SLEEVE
• 10886982308993 - NA: 2021-10-25 8MM CANNULATED STRAIGHT AWL WITH AO REAMER COUPLER
• 10886982309112 - NA: 2021-10-25 HANDLE
• 10886982309129 - NA: 2021-10-25 4.5 LCP PROTECTION SLEEVE
• 10886982309303 - NA: 2021-10-25 12MM CANNULATED DRILL BIT
• 10886982309310 - NA: 2021-10-25 13MM CANNULATED DRILL BIT
• 10886982311498 - NA: 2021-10-25 4.2MM CALIBRATED DRILL BIT
• 10886982311580 - NA: 2021-10-25 MEASURING DEVICE