FDA UDI In Commercial Distribution 🇺🇸 United States

PeelVue Pro

DI: 10615375010287 · Model: 37069 · Kerr Corporation
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
PeelVue Pro
Primary DI
10615375010287
Version / Model
37069
Company Name
Kerr Corporation
Labeler DUNS
199354556
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2019-07-01
Public Version
2
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
25141d75-1795-4db4-a709-328cbcec60ff

Device Description

Self-Sealing Sterilization Pouches

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JOJ Indicator, Physical/Chemical Sterilization Process
FRG Wrap, Sterilization

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Primary 10615375010287
Unit of Use 00615375010280
Package 20615375010284

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K162258 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 5.31" x 11.41" (135mm x 290mm)

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at ambient room temperature. Keep dry. Keep away from sunlight.