FDA UDI
In Commercial Distribution
🇺🇸 United States
endomina EZFuse suture
DI: 05425029282049
·
Model: endomina EZFuse suture
·
Endo Tools Therapeutics
Product Codes
1
GMDN Terms
1
Identifiers
8
Pkg Device Count
1
Basic Information
- Brand Name
- endomina EZFuse suture
- Primary DI
- 05425029282049
- Version / Model
- endomina EZFuse suture
- Company Name
- Endo Tools Therapeutics
- Labeler DUNS
- 400000750
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2026-03-19
- Public Version
- 1
- Public Version Date
- 2026-03-27
- Public Version Status
- New
- Public Device Record Key
- b67e1aa1-d53c-4b53-a272-8b36871204fe
Device Description
endomina EZFuse suture
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- MR Safe
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- Yes
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- Yes
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| OCW | Endoscopic Tissue Approximation Device | Gastroenterology, Urology | 876.1500 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 57874 | Suturing unit, single-use | A non-powered, hand-held device intended to pass sutures or a needle/suture assembly through tissues/prosthetic materials to facilitate suturing during an endoscopic and/or open surgical procedure; it may also knot, cut and/or tighten the sutures/ligature loop during or after placement. It typically consists of a shaft with hooks, catches, clasps, or forceps-like jaws at the distal end, and a proximal handle with controls. It typically has a pointed/cutting component to create a suture tunnel, and is loaded with the sutures or the suture is inserted through the shaft. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 05425029282643 | GS1 | secondary packaging | 6 | In Commercial Distribution | |
| Primary | 05425029282049 | GS1 | ||||
| Package | 05425029282346 | GS1 | Tertiary packaging | 12 | In Commercial Distribution | |
| Package | 05425029282131 | GS1 | Pallet | 8 | In Commercial Distribution | |
| Package | 05425029282452 | GS1 | Pallet | 12 | In Commercial Distribution | |
| Package | 05425029282766 | GS1 | Pallet | 16 | In Commercial Distribution | |
| Package | 05425029282384 | GS1 | Pallet | 20 | In Commercial Distribution | |
| Package | 05425029282889 | GS1 | Pallet | 24 | In Commercial Distribution |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K252400 | 000 |