FDA UDI Not in Commercial Distribution 🇺🇸 United States

IntroDucer

DI: 14048223000073 · Model: 001151-30L · Pajunk GmbH Medizintechnologie
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

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
IntroDucer
Primary DI
14048223000073
Version / Model
001151-30L
Catalog Number
001151-30L
Company Name
Pajunk GmbH Medizintechnologie
Labeler DUNS
317654283
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2016-09-01
Public Version
10
Public Version Date
2025-03-17
Public Version Status
Update
Public Device Record Key
0ba9d10d-36b7-4018-bd08-2a46dfac4460
Distribution End Date
2025-03-15

Device Description

1,0 x 30mm

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
MR Unsafe
Direct Marking Exempt
No
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
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
Primary 14048223000073
Unit of Use 04048223000076

Customer Contacts