FDA UDI In Commercial Distribution 🇺🇸 United States

HSW FINE-JECT®

DI: 04035873020875 · Model: 4710008025 · Henke-Sass, Wolf GmbH
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
HSW FINE-JECT®
Primary DI
04035873020875
Version / Model
4710008025
Catalog Number
4710008025
Company Name
Henke-Sass, Wolf GmbH
Labeler DUNS
317326411
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-13
Public Version
5
Public Version Date
2019-10-23
Public Version Status
Update
Public Device Record Key
b2922537-12fe-4e89-9384-563e2c08a30b

Device Description

HSW FINE-JECT® 0,80X25 MM / 21GX1" STERILE

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
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
No

Product Codes

Code Name
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
59230 Hypodermic needle, single-use

Identifiers

Type ID
Package 04035873020868
Primary 04035873020875
Unit of Use 04035873052357

Device Sizes

Type Value Unit Text
Length 25 Millimeter
Outer Diameter 0.80 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Protect from sunlight
Type
Special Storage Condition, Specify
Special Conditions
Keep dry