FDA UDI In Commercial Distribution 🇺🇸 United States

MICROTEK

DI: 00748426119660 · Model: 1 · Microtek Medical Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MICROTEK
Primary DI
00748426119660
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
2017-01-13
Public Version
3
Public Version Date
2023-03-22
Public Version Status
Update
Public Device Record Key
edbd547c-9066-4876-b63f-9619cf7fae6b

Device Description

FISCHER DRAPING SYSTEM, 1-EACH

Device Characteristics

Single Use
Yes
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
Yes
Has Serial Number
No
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
KKX Drape, surgical

GMDN Terms

Code Name
45021 Instrument/equipment drape, single-use, sterile

Identifiers

Type ID
Package 50748426119665
Primary 00748426119660

Customer Contacts

Storage Conditions

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