FDA UDI In Commercial Distribution 🇺🇸 United States

SURGIPLUS

DI: 74895237106039 · Model: 1 · KENPAX INTERNATIONAL LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
SURGIPLUS
Primary DI
74895237106039
Version / Model
1
Catalog Number
68-6201-B
Company Name
KENPAX INTERNATIONAL LIMITED
Labeler DUNS
686206765
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-02
Public Version
2
Public Version Date
2020-07-28
Public Version Status
Update
Public Device Record Key
aa72b004-1d70-4041-a76e-ec6de5757461

Device Description

PE Film Gown

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
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
OEA Non-Surgical Isolation Gown

GMDN Terms

Code Name
35492 Isolation gown, single-use

Identifiers

Type ID
Package 84895237106036
Primary 74895237106039