FDA UDI In Commercial Distribution 🇺🇸 United States

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DI: H816PM54101 · Model: PM5410 · CERTOL INTERNATIONAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
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Primary DI
H816PM54101
Version / Model
PM5410
Catalog Number
PM5410-1
Company Name
CERTOL INTERNATIONAL, LLC
Labeler DUNS
095153714
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2016-09-23
Public Version
6
Public Version Date
2022-11-01
Public Version Status
Update
Public Device Record Key
e9cacdfd-e2cc-4f8d-ab91-64719f9a6945

Device Description

Self-Sealing Sterilization Pouch/Packaging 5.25" x 10"

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Package H816PM54102
Primary H816PM54101
Unit of Use H816PM54100

Premarket Submissions

Submission Number Supplement Number
K953829 000