PressFT PGHS

GUDID 10845854901922

PressFT™ Drill Guide Spike Tip, Hip

Conmed Corporation

Surgical drill guide, reusable

• Primary Device ID: 10845854901922
• NIH Device Record Key: 73509e08-7b33-49fd-97a0-464f4c7117bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PressFT
• Version Model Number: PGHS
• Catalog Number: PGHS
• Company DUNS: 071595540
• Company Name: Conmed 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

Customer Support Contacts

• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM
• Phone: +1(800)237-0169
• Email: CUSTOMER_SERVICE@CONMED.COM

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY
• Special Storage Condition, Specify: Between 0 and 0 *KEEP DRY

Device Identifiers

Device Issuing Agency	Device ID
GS1	10845854901922 [Primary]

FDA Product Code

• NBH: Accessories, arthroscopic

Sterilization

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

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

[10845854901922]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-04-06
• Device Publish Date: 2019-07-24

On-Brand Devices [PressFT]

• 20845854036652: PRESSFT 2.6 W/TWO NO. 1 (4 METRIC) HI-FI SUTURES (1 WHITE/GREEN AND 1 WHITE/BLACK)
• 20845854036645: PRESSFT 2.6 W/ ONE NO. 2 (5 METRIC) HI-FI SUTURE, HIP (1 WHITE/BLACK)
• 20845854036638: PRESSFT 2.6 W/ONE NO. 2 (5 METRIC) HI-FI SUTURE (1 WHITE/BLACK)
• 20845854036621: PRESSFT 2.1 W/TWO NO. 0 (3.5 METRIC) HI-FI SUTURES (1 WHITE/BLACK AND 1 WHITE/BLUE)
• 20845854036614: PRESSFT 2.1 W/ ONE NO. 2 (5 METRIC) HI-FI SUTURE, HIP (1 WHITE/BLACK)
• 20845854036607: PRESSFT 2.1 W/ONE NO. 2 (5 METRIC) HI-FI SUTURE (1 WHITE/BLACK)
• 10845854901922: PressFT™ Drill Guide Spike Tip, Hip
• 10845854901892: PressFT™ Drill Guide Crown Tip, Hip
• 10845854027967: PressFT™ Drill Guide, Hip
• 10845854027912: PressFT™ Cannulated Obturator, Hip
• 20845854600075: PressFT™ Flex Drill Bit 2.6 mm, Hip
• 20845854600068: PressFT™ Flex Drill Bit 2.1 mm, Hip
• 20845854051167: PressFT™ Flex 2.6 GENESYS, Hip
• 20845854051150: PressFT™ Flex 2.1 PEEK, Hip
• 20845854051143: PressFT™ Flex 2.1 GENESYS, Hip
• 20845854051136: PressFT™ Flex 2.6 PEEK, Hip
• 10845854051191: PressFT™ Flex Obturator, Hip
• 10845854051184: PressFT™ Flex Curved Drill Guide, Hip
• 10845854051177: PressFT™ Flex Straight Drill Guide, Hip
• 10845854901915: PressFT™ Drill Bit 2.6mm, Hip
• 10845854901908: PressFT™ Drill Bit 2.1mm, Hip
• 30845854082359: PressFT™ Drill Bit 2.1mm, Hip
• 30845854082342: PressFT™ Drill Bit 2.6mm, Hip
• 30845854082335: PressFT™ Drill Guide Spike Tip, Hip
• 30845854082311: PressFT™ Drill Guide Crown Tip, Hip
• 10845854901939: PressFT™ Cannulated Obturator, Hip
• 10845854027950: PRESSFT DRILL BIT, 2.6MM, HIP
• 10845854027943: PRESSFT DRILL BIT, 2.6MM
• 10845854027936: PRESSFT DRILL BIT, 2.1MM, HIP
• 10845854027929: PRESSFT DRILL BIT, 2.1MM