FDA UDI In Commercial Distribution 🇺🇸 United States

Encompass

DI: 20612899005642 · Model: G-P9156 · Encompass Group, L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Encompass
Primary DI
20612899005642
Version / Model
G-P9156
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
2023-06-22
Public Version
1
Public Version Date
2023-06-30
Public Version Status
New
Public Device Record Key
c5205823-4231-43b3-bcf6-e46834cf2b97

Device Description

EVOLUTION PATIENT TOP, 3X,50EA TS EVO PATIENT TOP, NO POCKET/BINDING, GREEN, SBPP, 50 EA/CS

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
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
No

Product Codes

Code Name
FME Gown, Examination

GMDN Terms

Code Name
35092 Patient gown, single-use

Identifiers

Type ID
Primary 20612899005642

Customer Contacts