FDA UDI In Commercial Distribution 🇺🇸 United States

INTRODUCER

DI: 04048223052709 · Model: 021163-30L · Pajunk GmbH Medizintechnologie
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

Basic Information

Brand Name
INTRODUCER
Primary DI
04048223052709
Version / Model
021163-30L
Catalog Number
021163-30L
Company Name
Pajunk GmbH Medizintechnologie
Labeler DUNS
317654283
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2021-04-02
Public Version
6
Public Version Date
2024-02-16
Public Version Status
Update
Public Device Record Key
5d3d5f9c-ffc2-4181-a245-5da442346bd1
Distribution End Date
2024-05-25

Device Description

021163-30L

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
No

Product Codes

Code Name
MDM INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

GMDN Terms

Code Name
45018 Needle guide, single-use

Identifiers

Type ID
Unit of Use 04048223028797
Previous 14048223028794
Primary 04048223052709

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 65 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius