Tischler Morgan Biopsy Forceps Without Lock 13-042-01

GUDID G25013042010

A hand-held manual surgical instrument designed to obtain soft-tissue biopsy specimens from an open surgical wound or from within/near a large natural orifice (e.g., vagina, rectum) for histopathological examination; it is not intended for endoscopic or catheterized access. It is a metallic forceps-like instrument with a distal mechanism designed to bite/punch the biopsy sample and hold it for extraction when the handles are squeezed together. It is not designed for cutting bone (i.e., not a rongeur). This is a reusable device.

N S SURGICAL COMPANY

Open-surgery biopsy forceps, reusable

• Primary Device ID: G25013042010
• NIH Device Record Key: f7e966be-fc47-48c7-9dbf-34b4e4fb6356
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tischler Morgan Biopsy Forceps Without Lock
• Version Model Number: 13-042-01
• Catalog Number: 13-042-01
• Company DUNS: 645681649
• Company Name: N S SURGICAL COMPANY
• 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: false
• OTC Over-The-Counter: false

Device Dimensions

• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0
• Length: 23 Centimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	G25013042010 [Primary]

FDA Product Code

• HFB: Forceps, Biopsy, Gynecological

Sterilization

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

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

[G25013042010]

Moist Heat or Steam Sterilization;Ultraviolet Light;Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-05-08
• Device Publish Date: 2023-04-29

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