FDA UDI In Commercial Distribution 🇺🇸 United States

Capella™

DI: 00821329400322 · Model: 1012868‐004 · Greatbatch Ltd
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Capella™
Primary DI
00821329400322
Version / Model
1012868‐004
Catalog Number
MK5181
Company Name
Greatbatch Ltd
Labeler DUNS
968623467
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-06
Public Version
3
Public Version Date
2019-06-07
Public Version Status
Update
Public Device Record Key
fb471b19-ec58-4dca-bb79-f1ebee2327ee

Device Description

5 French Coaxial Micro-Introducer Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DYB Introducer, Catheter

GMDN Terms

Code Name
58865 Vascular catheter introduction set, nonimplantable

Identifiers

Type ID
Package 10821329400329
Primary 00821329400322

Device Sizes

Type Value Unit Text
Device Size Text, specify .018" [.47 mm] SS/SS Straight Tip Guidewire 45.0 cm
Device Size Text, specify Needle, .55 mm ID, 0.9 mm OD, Echo Tip, 21 Ga. x 69.9 mm
Device Size Text, specify Dilator 0.4 mm ID, 1.1 mm OD, 11.8 cm Length
Device Size Text, specify 5 F Sheath 0.9 mm ID, 9.3 cm Length
Length 9.3 Centimeter