FDA UDI In Commercial Distribution 🇺🇸 United States

Tissue-Tek Xpress® x120

DI: 00615233081667 · Model: 7730 · SAKURA FINETEK U.S.A., INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tissue-Tek Xpress® x120
Primary DI
00615233081667
Version / Model
7730
Catalog Number
7730
Company Name
SAKURA FINETEK U.S.A., INC.
Labeler DUNS
179135769
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-15
Public Version
1
Public Version Date
2019-12-23
Public Version Status
New
Public Device Record Key
351f17b5-4e7a-4650-8bfa-8de017a06ebd

Device Description

Processing Reagent Set

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LDZ FIXATIVE, ALCOHOL CONTAINING
KEO FORMULATIONS, PARAFFIN, ALL

GMDN Terms

Code Name
63938 Histology tissue processing reagent kit IVD

Identifiers

Type ID
Primary 00615233081667

Customer Contacts