FDA UDI In Commercial Distribution 🇺🇸 United States

SURGICAL STERILE DRAPE

DI: 08056646501861 · Model: 12.T1754.00 · OMNIA SRL
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
SURGICAL STERILE DRAPE
Primary DI
08056646501861
Version / Model
12.T1754.00
Company Name
OMNIA SRL
Labeler DUNS
447696675
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2016-09-11
Public Version
6
Public Version Date
2021-12-22
Public Version Status
Update
Public Device Record Key
f6bc600a-f90b-4316-9294-f4dcf1f935df

Device Description

LIQUID REPELLENT DRAPE CM 67X75 WITH ADHESIVE HOLE CM 6X9 BLUE - SONTARA - BLUE

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KKX Drape, Surgical

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Primary 08056646501861
Unit of Use 08056646501854

Customer Contacts