FDA UDI In Commercial Distribution 🇺🇸 United States

SPROTTE®

DI: 14048223014018 · Model: 001152-30C · Pajunk GmbH Medizintechnologie
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
SPROTTE®
Primary DI
14048223014018
Version / Model
001152-30C
Catalog Number
001152-30C
Company Name
Pajunk GmbH Medizintechnologie
Labeler DUNS
317654283
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2016-08-30
Public Version
4
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
fcfbada6-9d5e-4a21-b3bf-3958c656ab48
Distribution End Date
2025-03-15

Device Description

SPROTTE® 22G x 3 1/2", w. stylet 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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
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
BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

GMDN Terms

Code Name
35212 Spinal needle, single-use

Identifiers

Type ID
Primary 14048223014018
Unit of Use 04048223014011

Customer Contacts