Primary Device ID | H816PM24402 |
NIH Device Record Key | 9a30676b-aa4f-4b7c-becc-8d1f793605e8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ProView plus |
Version Model Number | PM2440 |
Catalog Number | PM2440-1 |
Company DUNS | 095153714 |
Company Name | CERTOL INTERNATIONAL, LLC |
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 | false |
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 Issuing Agency | Device ID |
---|---|
HIBCC | H816PM24400 [Unit of Use] |
HIBCC | H816PM24401 [Primary] |
HIBCC | H816PM24402 [Package] Contains: H816PM24401 Package: Case Box [12 Units] In Commercial Distribution |
KCT | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2016-09-23 |
H816PM75132 | Self-Sealing Sterilization Pouch/Packaging 7.5" x 13" |
H816PM54102 | Self-Sealing Sterilization Pouch/Packaging 5.25" x 10" |
H816PM35902 | Self-Sealing Sterilization Pouch/Packaging 3.5" x 9" |
H816PM35542 | Self-Sealing Sterilization Pouch/Packaging 3.5" X 5.25" |
H816PM27902 | Self Sealing Sterilization Pouch/Packaging 2 3/4" X 9" |
H816PM24402 | Self Sealing Sterilization Pouch/Packaging 2 1/4" x 4" |
H816PM13191 | Self-Sealing Sterilization Pouch/Packaging 13" X 18" |
H816PM13181 | Self-Sealing Sterilization Pouch/Packaging 13" X 18" |
H816PM10161 | Self-Sealing Sterilization Pouch/Packaging 10" X 16" |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PROVIEW PLUS 88005171 not registered Live/Pending |
ProSOC, Inc. 2018-06-18 |