FDA UDI In Commercial Distribution 🇺🇸 United States

ANGIO-SEAL

DI: 00389701011820 · Model: 610130 · TERUMO MEDICAL CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
ANGIO-SEAL
Primary DI
00389701011820
Version / Model
610130
Catalog Number
610130
Company Name
TERUMO MEDICAL CORPORATION
Labeler DUNS
962520628
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-20
Public Version
5
Public Version Date
2021-02-05
Public Version Status
Update
Public Device Record Key
a4389781-d0b8-49e4-bfb6-82ed2c2f3242

Device Description

ANGIO-SEAL VIP Vascular Closure Device

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
No
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
MGB Device, hemostasis, vascular

GMDN Terms

Code Name
60710 Femoral artery closure plug/patch, collagen

Identifiers

Type ID
Package 50389701011825
Package 30389701011821
Primary 00389701011820

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 6 French

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 25 Degrees Celsius
Type
Special Storage Condition, Specify
Special Conditions
Keep dry and Keep away from sunlight, including UV light. Do not use if temperature indicator dot has changed from light gray to dark gray or black.