Finch Excision Clamp, Hollow Jaw, 235mm O/L, 95mm Jaw

GUDID 05056405502880

PLATTS & NISBETT LIMITED

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: 05056405502880
• NIH Device Record Key: 2823ca0f-a816-4796-8796-e6a52f0e20e0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Finch Excision Clamp, Hollow Jaw, 235mm O/L, 95mm Jaw
• Version Model Number: PN0390
• Company DUNS: 290712512
• Company Name: PLATTS & NISBETT LIMITED
• 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	05056405502880 [Primary]

FDA Product Code

• HXD: Clamp

Sterilization

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

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

[05056405502880]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-23
• Device Publish Date: 2024-04-15

Devices Manufactured by PLATTS & NISBETT LIMITED

• 05056405502880 - Finch Excision Clamp, Hollow Jaw, 235mm O/L, 95mm Jaw: 2024-04-23
• 05056405502880 - Finch Excision Clamp, Hollow Jaw, 235mm O/L, 95mm Jaw: 2024-04-23
• 05056405504235 - Smith Petersen Osteotome, Curved, 205mm O/L, 13mm Width: 2024-03-15
• 05056405508868 - SPAIRE Hohmann Retractor, Angled, 18mm: 2023-10-31
• 05056405508875 - SPAIRE Iliac Wing Retractor: 2023-10-31
• 05056405508882 - SPAIRE T Handle Retractor with Ischial/Iliac Pins: 2023-10-31
• 05056405508899 - SPAIRE Reamer Detachment Forceps: 2023-10-31
• 05056405508905 - SPAIRE Anterior Retractor, Double Angled, 25mm: 2023-10-31
• 05056405509049 - SPAIRE Inferior Retractor, 22mm: 2023-10-31