FDA UDI In Commercial Distribution 🇺🇸 United States

MICROTEK

DI: 50748426104234 · Model: 1 · Microtek Medical Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MICROTEK
Primary DI
50748426104234
Version / Model
1
Company Name
Microtek Medical Inc.
Labeler DUNS
106908437
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-27
Public Version
4
Public Version Date
2023-03-22
Public Version Status
Update
Public Device Record Key
91c1aaea-c6f3-4052-b4e5-2a2c1e5c89bd

Device Description

VITALVAC - 230V, 1-CASE

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FYD APPARATUS, EXHAUST, SURGICAL

GMDN Terms

Code Name
48027 Surgical fluid/smoke waste management system suction unit

Identifiers

Type ID
Primary 50748426104234

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K001082 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store under normal warehouse conditions.