FDA UDI In Commercial Distribution 🇺🇸 United States

PeelVue Pro

DI: 10615375011819 · Model: 37149 · Kerr Corporation
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
200

Basic Information

Brand Name
PeelVue Pro
Primary DI
10615375011819
Version / Model
37149
Company Name
Kerr Corporation
Labeler DUNS
199354556
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2020-12-31
Public Version
1
Public Version Date
2021-01-08
Public Version Status
New
Public Device Record Key
43c4c42c-8e6e-4d14-819e-0964946c07bc

Device Description

Self-Sealing Sterilization Pouches (Case has a different SKU number, i.e. 37151)

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

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Unit of Use 00615375011812
Primary 10615375011819
Package 20615375011816

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K162258 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 90mm x 230mm

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at Ambient Room Temperature, Keep Dry, Keep away from sunlight