FDA UDI In Commercial Distribution 🇺🇸 United States

SPROTTE®

DI: 04048223109168 · Model: 521151-29A · Pajunk GmbH Medizintechnologie
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
25

Basic Information

Brand Name
SPROTTE®
Primary DI
04048223109168
Version / Model
521151-29A
Catalog Number
521151-29A
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
3
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
73d03e89-2c8c-4bd8-96b7-0e94634d5af4

Device Description

Needle

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
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
BSP NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

GMDN Terms

Code Name
35212 Spinal needle, single-use

Identifiers

Type ID
Unit of Use 04048223001745
Previous 14048223001742
Primary 04048223109168

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 0.5 Millimeter
Length 90.0 Millimeter

Storage Conditions

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