FDA UDI In Commercial Distribution 🇺🇸 United States

EndoArmor™ +

DI: 00191506005917 · Model: M00501971 · BOSTON SCIENTIFIC CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
EndoArmor™ +
Primary DI
00191506005917
Version / Model
M00501971
Catalog Number
M00501971
Company Name
BOSTON SCIENTIFIC CORPORATION
Labeler DUNS
021717889
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2022-05-13
Public Version
1
Public Version Date
2022-05-23
Public Version Status
New
Public Device Record Key
ca213f7f-1307-4b2c-a066-85ef3d5c4da1

Device Description

AAMI LEVEL 3 Surgical Gown

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
FYA GOWN, SURGICAL

GMDN Terms

Code Name
35091 Surgical gown, single-use

Identifiers

Type ID
Package 00191506005924
Primary 00191506005917
Unit of Use 00191506005900