Vermed

Basic Information

• Brand Name: Vermed
• Primary DI: 00009336006595
• Version / Model: SHRP5.4 QT PHARMA WALL UNIT
• Catalog Number: 32028097
• Company Name: GRAPHIC CONTROLS ACQUISITION CORP
• Labeler DUNS: 002111896
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2017-01-24
• Public Version: 4
• Public Version Date: 2023-08-18
• Public Version Status: Update
• Public Device Record Key: 55df3666-490f-45ce-8959-8b204bb30827

Device Description

SHRP5.4 QT PHARMA WALL UNIT

Device Characteristics

• Single Use: No
• Prescription Use (Rx): No
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: Yes
• MRI Safety: MR Unsafe
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
MMK	Container, Sharps	General Hospital	880.5570	2

GMDN Terms

Code	Name	Definition	Implantable	Status
36021	Cytotoxic waste container	A container made of metal, hard plastic and/or cardboard designed for the safe deposit, collection and storage of cytotoxic materials (e.g., chemotherapy/antineoplastic drugs). It is typically used with a liner or a sealed leak proof bag, and has a lid for that allows temporary and final closure options; the lid typically includes a seal to prevent leakage. It is identified with a cytotoxic biohazard symbol on its labelling and sent to an appropriate waste treatment plant for disposal when filled to the recommended level.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	70009336006594	GS1	Pallet	28	In Commercial Distribution
Package	50009336006590	GS1	Case	12	In Commercial Distribution
Primary	00009336006595	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]

Premarket Submissions

Submission Number	Supplement Number
K071517	000