AUTOCLAVE TAPE

GUDID D89260705600591

MAXILL, INC.

Chemical/physical sterilization process indicator Chemical/physical sterilization process indicator Chemical/physical sterilization process indicator Chemical/physical sterilization process indicator Chemical/physical sterilization process indicator Chemical/physical sterilization process indicator Chemical/physical sterilization process indicator Chemical/physical sterilization process indicator Chemical/physical sterilization process indicator Chemical/physical sterilization process indicator Chemical/physical sterilization process indicator

Primary Device ID	D89260705600591
NIH Device Record Key	ae582d82-02a5-4502-8af1-71f7772e283d
Commercial Distribution Status	In Commercial Distribution
Brand Name	AUTOCLAVE TAPE
Version Model Number	6070560059
Company DUNS	079343581
Company Name	MAXILL, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
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	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 Identifiers

Device Issuing Agency	Device ID
HIBCC	D89260705600590 [Primary]
HIBCC	D89260705600591 [Package] Contains: D89260705600590 Package: CASE [54 Units] In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K171823

FDA Product Code

JOJ	Indicator, Physical/Chemical Sterilization Process

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	2022-09-27
Device Publish Date	2022-09-19

On-Brand Devices [AUTOCLAVE TAPE]

D89260705600591	6070560059
D89260705600581	6070560058
D89260705600571	6070560057