FDA UDI In Commercial Distribution 🇺🇸 United States

Maytex Nupack

DI: D806MBFC1 · Model: MBFC · MAYTEX CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Maytex Nupack
Primary DI
D806MBFC1
Version / Model
MBFC
Company Name
MAYTEX CORPORATION
Labeler DUNS
196642151
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-03
Public Version
2
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
1abf2698-d471-4217-a391-a42658aa431f

Device Description

Barrier Film Clear

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
No
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
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

GMDN Terms

Code Name
13735 Sterilization packaging, single-use

Identifiers

Type ID
Primary D806MBFC1

Premarket Submissions

Submission Number Supplement Number
K162258 000