FDA UDI In Commercial Distribution 🇺🇸 United States

MICROTEK

DI: 00748426011100 · Model: 1 · Microtek Medical Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MICROTEK
Primary DI
00748426011100
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
2016-11-04
Public Version
6
Public Version Date
2023-03-22
Public Version Status
Update
Public Device Record Key
f3d647f6-65ad-4620-9546-9c06a66e1b93

Device Description

ADULT CRANIOTOMY DRAPE, LATEX FREE, 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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
KKX Drape, surgical

GMDN Terms

Code Name
47783 Patient surgical drape, single-use

Identifiers

Type ID
Package 50748426011105
Primary 00748426011100

Customer Contacts

Storage Conditions

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