BENSON UNIVERSAL IMPLANT SIZER

GUDID 00844505014328

Grace Medical, Inc.

Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable Surgical implant/trial-implant/sizer holder, reusable

• Primary Device ID: 00844505014328
• NIH Device Record Key: 40278215-a7a2-4f5f-a0f1-45f2af6b0f92
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BENSON UNIVERSAL IMPLANT SIZER
• Version Model Number: 916
• Company DUNS: 030849173
• Company Name: Grace Medical, Inc.
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00844505014328 [Primary]

FDA Product Code

• JYJ: Gauge, Measuring

Sterilization

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

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

[00844505014328]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-05
• Device Publish Date: 2023-09-27

Devices Manufactured by Grace Medical, Inc.

• 10844505014394 - TOUMA VENT TUBE W/ TAB: 2024-01-31 MODIFIED TOUMA VENT TUBE W/ TAB 1.27MM ID SILICONE
• 10844505014004 - ARMSTRONG VENT TUBE: 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID FLUOROPLASTIC 5 PACK
• 10844505014042 - ARMSTRONG VENT TUBE: 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID BLUE FLUOROPLASTIC 5 PACK
• 10844505014080 - ARMSTRONG VENT TUBE: 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID FLUOROPLASTIC 10 PACK
• 10108445050141 - ARMSTRONG VENT TUBE: 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID BLUE FLUOROPLASTIC 10 PACK
• 10844505014165 - ARMSTRONG VENT TUBE: 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID FLUOROPLASTIC 30 PACK
• 10844505014189 - ARMSTRONG VENT TUBE: 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID BLUE FLUOROPLASTIC 30 PACK
• 10844505014240 - ARMSTRONG VENT TUBE: 2023-12-12 ARMSTRONG VENT TUBE 1.14MM ID FLUOROPLASTIC 60 PACK