AccessGUDID - DEVICE: SPROTTE® (04048223049761)

GUDID

Device Identifier (DI) Information

Brand Name: SPROTTE®
Version or Model: 001163-30D
Commercial Distribution Status: Not in Commercial Distribution
Catalog Number: 001163-30D
Company Name: Pajunk GmbH Medizintechnologie

Primary DI Number: 04048223049761
Issuing Agency: GS1
Commercial Distribution End Date: January 17, 2025
Device Count: 25
Labeler D-U-N-S® Number*: 317654283 *Terms of Use
Previous DI: 14048223030292

Device Description: Distal Tip: SPROTTE® Proximal End: ISO 80369-6

Device Characteristics

What MRI safety information does the labeling contain?	Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437):	No
Device labeled as "Not made with natural rubber latex":	No
For Single-Use:	Yes
Prescription Use (Rx):	No
Over the Counter (OTC):	No
Kit:	No
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No

GMDN

[?]

GMDN Term Code	GMDN Term Name	GMDN Term Definition	GMDN Term Status [?]	Implantable?
35212	Spinal needle, single-use	A sharp bevel-edged, hollow tubular instrument designed for short-term use to withdraw a sample of cerebrospinal fluid (CSF), assist introduction of a spinal guidewire or catheter (e.g., lumboperitoneal shunt, intrathecal catheter), and/or deliver contrast media and/or anaesthetic or analgesic agents intrathecally (subarachnoid) or into a vertebral disc, either directly or using the needle-through-needle technique. It is typically fenestrated, spring-tipped, and made of metal and/or plastic materials; some types may be semi-rigid and include a stylet for support during handling. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
BSP	NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
Premarket Submission Number Not Available/Not Released

Device Exempt from Premarket Submission: No CLOSE

Sterilization

Device Packaged as Sterile: Yes
Requires Sterilization Prior to Use: No

Sterilization Method [?]
No Sterilization Methods Found

Storage and Handling

[?]

Storage and Handling
Storage Environment Temperature: between 10 and 30 Degrees Celsius
Storage Environment Humidity: between 10 and 65 Percent (%) Relative Humidity

Clinically Relevant Size

[?]

Size Type Text
Outer Diameter: 0.55 Millimeter
Length: 25.0 Millimeter

Device Record Status

Public Device Record Key: d4a477e2-bfe7-49c4-8209-c643257e2386
Public Version Date: January 17, 2025
Public Version Number: 6
DI Record Publish Date: April 02, 2021