GUDID 00850005084099

Rochester-Pean Forceps, 6"

PACIFIC INSTRUMENTS, INC.

Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable Surgical soft-tissue manipulation forceps, scissors-like, reusable

• Primary Device ID: 00850005084099
• NIH Device Record Key: 6cc7718f-b2ce-41be-ac59-a91c43763488
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: PI-3360
• Company DUNS: 621872006
• Company Name: PACIFIC INSTRUMENTS, 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850005084099 [Primary]

FDA Product Code

• HTD: Forceps

Sterilization

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

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

[00850005084099]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-28
• Device Publish Date: 2024-05-20

Devices Manufactured by PACIFIC INSTRUMENTS, INC.

• 00850005084877 - NA: 2024-06-10 3.7x5.5mm Cup Curette, Angled Up 90°
• 00850005084075 - NA: 2024-05-28 Dental Pick / 5x8mm Cup Curette
• 00850005084099 - NA: 2024-05-28Rochester-Pean Forceps, 6"
• 00850005084099 - NA: 2024-05-28 Rochester-Pean Forceps, 6"
• 00850005084167 - NA: 2024-04-25 Cervical Spreader
• 00850005084693 - NA: 2024-04-05 Power Bender for up to 5.5mm Rods
• 00850005084686 - NA: 2024-03-28 8x11mm Cup Curette, Angled Up
• 00850005084679 - NA: 2024-03-27 Lamina Distractor
• 00850005084082 - NA: 2024-03-26 Plate Bending Pliers for Forearm Plate