FDA UDI In Commercial Distribution 🇺🇸 United States

Encompass

DI: 00609953927640 · Model: CD0403 · Encompass Group, L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Encompass
Primary DI
00609953927640
Version / Model
CD0403
Company Name
Encompass Group, L.L.C.
Labeler DUNS
121788819
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-18
Public Version
5
Public Version Date
2023-05-10
Public Version Status
Update
Public Device Record Key
883ff77e-e705-4397-9140-2c0b9d527319

Device Description

CYSTO SHEET 40X40 T180 JADE

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KKX Drape, surgical

GMDN Terms

Code Name
47780 Patient surgical drape, reusable

Identifiers

Type ID
Package 50609953927645
Primary 00609953927640

Customer Contacts