AccessGUDID - DEVICE: Lockado(TM) Repositionable Hemostasis Clip (06932503530996)

GUDID

Device Identifier (DI) Information

Brand Name: Lockado(TM) Repositionable Hemostasis Clip
Version or Model: LOCK-F-26-195-C-N
Commercial Distribution Status: In Commercial Distribution
Catalog Number:
Company Name: Micro-Tech (Nanjing) Co., Ltd.

Primary DI Number: 06932503530996
Issuing Agency: GS1
Commercial Distribution End Date:
Device Count: 1
Labeler D-U-N-S® Number*: 530269083 *Terms of Use

Device Description: Open width16±2mm the max OD of insertion part 2.6mm working length 1950mm coated, single pickling wire Open width16±2mm the max OD of insertion part 2.6mm working length 1950mm coated, 2 pcs in the box

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":	Yes
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?
61208	Gastrointestinal endoscopic clip, long-term, non-bioabsorbable	A non-bioabsorbable clip intended to be implanted long-term (>30 days) within the gastrointestinal (GI) tract during an endoscopic procedure for endoscopic marking, haemostasis, tissue approximation, closure of luminal perforations, treating mucosal/submucosal defects, and/or as part of bariatric procedures. It is a metallic device with a clasping mechanism; a disposable applicator may be included.	Active	true

FDA Product Code

[?]

Product Code	Product Code Name
PKL	Hemostatic Metal Clip For The Gi Tract

FDA Premarket Submission

FDA Premarket Submission Number [?]	Supplement Number [?]
K202333	000

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
Length: 195 Centimeter
Outer Diameter: 2.6 Millimeter

Device Record Status

Public Device Record Key: bc47f349-4c80-4967-a3c6-0e8be58ae3b6
Public Version Date: October 11, 2024
Public Version Number: 3
DI Record Publish Date: December 31, 2022

Alternative and Additional Identifiers Additional Identifiers

Package DI

[?]

Package DI Number	Quantity per Package	Contains DI Package	Package Status	Package Type
16932503530993	10	06932503530996	In Commercial Distribution	BOX
26932503530990	10	16932503530993	In Commercial Distribution	CASE
56932503530991	2	06932503530996	In Commercial Distribution	BOX
66932503530998	25	56932503530991	In Commercial Distribution	CASE