Kelly Forceps Straight 5.5" GI-S-242

GUDID B928GIS2420

Kelly Forceps Straight Size 5.5"

GARANA INDUSTRIES PVT LTD

Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use Surgical soft-tissue manipulation forceps, scissors-like, single-use

• Primary Device ID: B928GIS2420
• NIH Device Record Key: 526d53e0-d6ef-4b58-9d78-46150fba6a0b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kelly Forceps Straight 5.5"
• Version Model Number: GI-S-242
• Catalog Number: GI-S-242
• Company DUNS: 645568952
• Company Name: GARANA INDUSTRIES PVT LTD
• Device Count: 500
• DM Exempt: true
• 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: true
• 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
HIBCC	B928GIS2420 [Unit of Use]
HIBCC	B928GIS2421 [Primary]

FDA Product Code

• HRQ: Hemostat

Sterilization

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

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

[B928GIS2420]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-02-16
• Device Publish Date: 2021-02-08