AccessGUDID - DEVICE: LoFric® Origo™ (07333387043319)

GUDID

Device Identifier (DI) Information

Brand Name: LoFric® Origo™
Version or Model: 44312
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 4431240
Company Name: Wellspect AB

Primary DI Number: 07333387043319
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 351118942 *Terms of Use
Previous DI: 07392532158292

Device Description: Single Use Urinary Catheter with salt solution. LoFric Origo, Nelaton 40cm CH12 / Nelaton 16" 12FR, Sterile device.

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):	Yes
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?
45605	Single-administration urethral catheterization kit, single-use	A sterile collection of devices that includes a urological catheter (with or without a urine drainage bag), a cap, and other related accessories intended for one-time, self-urinary catheterization. The catheter is inserted through the urethra by the patient to provide urine drainage. This is a single-use device.	Active	false

FDA Product Code

[?]

Product Code	Product Code Name
EZD	Catheter, straight

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
Special Storage Condition, Specify: Store in a dry place at room temperature

Clinically Relevant Size

[?]

Size Type Text
Length: 16 Inch
Catheter Gauge: 12 French

Device Record Status

Public Device Record Key: b817af5c-061f-4b9b-b151-43cdfe5241fd
Public Version Date: September 27, 2023
Public Version Number: 2
DI Record Publish Date: September 18, 2023

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Status
07333387004730	4	07333387004723	In Commercial Distribution
07333387004723	30	07333387043319	In Commercial Distribution
07333387004570	5	07333387043319	In Commercial Distribution