AccessGUDID - DEVICE: Stat Tack (05708932479462)

GUDID

Device Identifier (DI) Information

Brand Name: Stat Tack
Version or Model: 501260
Commercial Distribution Status: In Commercial Distribution
Catalog Number: 501260
Company Name: Coloplast A/S

Primary DI Number: 05708932479462
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 305524696 *Terms of Use

Device Description: Fixation 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?
45613	Surgical binding material anchor set	A collection of devices designed to implant a non-bioabsorbable fixation anchor into ligaments or other soft tissues to serve as a site of attachment for surgical binding materials (e.g., mesh, sutures). The set typically consists of non-bioabsorbable fixation anchors, possibly contained within a cartridge, and a mechanical applicator used to hold, position, and insert each anchor into the target tissue; and possibly a drill or punch to create the hole to deliver the anchor. This is a single-patient device.	Obsolete	false

FDA Product Code

[?]

Product Code	Product Code Name
GDW	STAPLE, IMPLANTABLE

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
No storage/handling found

Clinically Relevant Size

[?]

Size Type Text
Outer Diameter: 5 Millimeter

Device Record Status

Public Device Record Key: 644a9478-1ee9-49fa-9b98-9dd74daa909d
Public Version Date: March 29, 2018
Public Version Number: 2
DI Record Publish Date: March 29, 2016

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Discontinue Date	Package Status	Package Type
No Package DIs found

Secondary DI

[?]

Issuing Agency [?]	Secondary DI Number
No Secondary DIs found

Unit of Use DI

[?]

Unit of Use DI Number: No Unit of Use DI Numbers Found CLOSE

Direct Marking (DM)

[?]

Device Subject to Direct Marking (DM), but Excepted: No
DM DI Different from Primary DI: No
DM DI Number: None
CLOSE

Production Identifier(s) in UDI

[?]

Lot or Batch Number: Yes
Serial Number: No
Expiration Date: Yes
Manufacturing Date: No
Donation Identification Number: No CLOSE

Customer Contact

[?]

Phone: +1(800)258-3476
Email: urology@coloplast.com

MENU
- Home
- About
- News
- API
- Download
- Help

FDA TOOLS & RESOURCES