FDA UDI In Commercial Distribution 🇺🇸 United States

SPROTTE®

DI: 04048223098752 · Model: 321151-30F · Pajunk GmbH Medizintechnologie
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
SPROTTE®
Primary DI
04048223098752
Version / Model
321151-30F
Catalog Number
321151-30F
Company Name
Pajunk GmbH Medizintechnologie
Labeler DUNS
317654283
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-07-15
Public Version
1
Public Version Date
2025-07-23
Public Version Status
New
Public Device Record Key
b563dd59-780e-4187-9f59-0aa37ebe230b

Device Description

SPROTTE® 18G x 4 3/4" (120mm) with Introducer and wings

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
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
Package 04048223108604
Primary 04048223098752

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
20 – 65 Percent (%) Relative Humidity