FDA UDI In Commercial Distribution 🇺🇸 United States

Hemashield

DI: 00384401017950 · Model: M00202019579P0 · INTERVASCULAR SAS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hemashield
Primary DI
00384401017950
Version / Model
M00202019579P0
Catalog Number
M00202019579P0
Company Name
INTERVASCULAR SAS
Labeler DUNS
382174019
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-11
Public Version
4
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
031fbd06-d428-4414-918b-158482244e8f

Device Description

Hemashield Platinum Finesse Ultra-Thin Knitted Cardiovascular Patch

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
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DXZ Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene

GMDN Terms

Code Name
35273 Cardiovascular patch, animal-derived

Identifiers

Type ID
Primary 00384401017950

Customer Contacts

Phone
+33442084646

Premarket Submissions

Submission Number Supplement Number
K962342 000

Device Sizes

Type Value Unit Text
Length 7.6 Centimeter
Width 0.8 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Controlled Room Temperature