FDA UDI In Commercial Distribution 🇺🇸 United States

Tissue-Tek® Accu-Edge®

DI: 04902470058252 · Model: 4687 · SAKURA FINETEK U.S.A., INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tissue-Tek® Accu-Edge®
Primary DI
04902470058252
Version / Model
4687
Catalog Number
4687
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
2020-03-31
Public Version
3
Public Version Date
2020-08-20
Public Version Status
Update
Public Device Record Key
1f38e108-bc63-417a-a2ba-e4d098ba2a1b

Device Description

Microtome Blade System

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GES BLADE, SCALPEL

GMDN Terms

Code Name
42439 Microtome blade IVD, reusable

Identifiers

Type ID
Primary 04902470058252

Customer Contacts