STERI-SOX MULTI-CHANNEL STERILIZATION POUCHES

GUDID D89260705601492

MAXILL, INC.

Sterilization packaging, single-use Sterilization packaging, single-use Sterilization packaging, single-use Sterilization packaging, single-use Sterilization packaging, single-use Sterilization packaging, single-use Sterilization packaging, single-use Sterilization packaging, single-use Sterilization packaging, single-use Sterilization packaging, single-use Sterilization packaging, single-use

Primary Device ID	D89260705601492
NIH Device Record Key	25a09078-0146-4a38-aec7-43b87f4eccb8
Commercial Distribution Status	In Commercial Distribution
Brand Name	STERI-SOX MULTI-CHANNEL STERILIZATION POUCHES
Version Model Number	6070560149
Company DUNS	079343581
Company Name	MAXILL, INC.
Device Count	200
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	D89260705601490 [Unit of Use]
HIBCC	D89260705601491 [Primary]
HIBCC	D89260705601492 [Package] Contains: D89260705601491 Package: CASE [2000 Units] In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K202462

FDA Product Code

FRG	Wrap, Sterilization

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 [STERI-SOX MULTI-CHANNEL STERILIZATION POUCHES]

D89260705601492	6070560149
D89260705601482	6070560148
D89260705601472	6070560147