FDA UDI In Commercial Distribution 🇺🇸 United States

MicroMyst

DI: 10381780000112 · Model: 205000DS · Integra Lifesciences Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MicroMyst
Primary DI
10381780000112
Version / Model
205000DS
Catalog Number
205000DS
Company Name
Integra Lifesciences Corporation
Labeler DUNS
083171244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-29
Public Version
5
Public Version Date
2023-05-15
Public Version Status
Update
Public Device Record Key
2a94b651-1382-4d8b-9f87-8008ed26d8e8

Device Description

MicroMyst Applicator (14cm) 5 pack - for use with Flow Regulator

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
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
FMF Syringe, Piston

GMDN Terms

Code Name
44830 Open-surgery adhesive/sealant applicator, dual-channel

Identifiers

Type ID
Package 30381780000116
Primary 10381780000112

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K082454 000

Device Sizes

Type Value Unit Text
Length 14 Centimeter