fold-n-hold 1010

GUDID 10850045406292

Pouch 10 pocket unit

General Hospital Supply Corp

Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use, non-sterile Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use Surgical instrument guard, single-use

• Primary Device ID: 10850045406292
• NIH Device Record Key: 5c6f396a-f4f4-4ac4-aaca-4affe70c9e05
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: fold-n-hold
• Version Model Number: 1010
• Catalog Number: 1010
• Company DUNS: 055852834
• Company Name: General Hospital Supply Corp
• Device Count: 100
• 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: true
• Lot Batch: false
• 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	00850045406295 [Primary]
GS1	10850045406292 [Unit of Use]

FDA Product Code

• LRP: Tray, Surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-28
• Device Publish Date: 2022-09-20

On-Brand Devices [fold-n-hold]

• 10850045406292: Pouch 10 pocket unit
• 10850045406285: Pouch 4 x 17
• 10850045406278: Pouch 5 x 5
• 10850045406261: Pouch 8 x 12
• 10850045406254: Pouch 8 x 9.5