Linear Stapler

GUDID 06939282458633

B. J. ZH. F. Panther Medical Equipment Co., Ltd.

Open-surgery manual linear stapler, single-use

• Primary Device ID: 06939282458633
• NIH Device Record Key: 0be7e2a8-064f-4209-ba99-58e234516168
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Linear Stapler
• Version Model Number: FLSLF45 3.5
• Company DUNS: 559966539
• Company Name: B. J. ZH. F. Panther Medical Equipment Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• 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	06939282458633 [Primary]

FDA Product Code

• GDW: Staple, Implantable

Sterilization

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

[06939282458633]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-05-07
• Device Publish Date: 2018-04-04

On-Brand Devices [Linear Stapler]

• 06939282458688: FLSLF90 4.8
• 06939282458671: FLSLF90 3.5
• 06939282458664: FLSLF60 4.8
• 06939282458657: FLSLF60 3.5
• 06939282458640: FLSLF45 4.8
• 06939282458633: FLSLF45 3.5
• 06939282458626: FLSLF30 4.8
• 06939282458619: FLSLF30 3.5
• 06939282458602: FLSLF30 2.5
• 06939282458572: FLSL90 4.8
• 06939282458565: FLSL90 3.5
• 06939282458558: FLSL60 4.8
• 06939282458541: FLSL60 3.5
• 06939282458534: FLSL45 4.8
• 06939282458527: FLSL45 3.5
• 06939282458510: FLSL30 4.8
• 06939282458503: FLSL30 3.5