FDA UDI
In Commercial Distribution
🇺🇸 United States
Disposable Endoscope Injection Needle
DI: 06936603226544
·
Model: FTL-IN-24-230-19-5
·
Yangzhou Fartley Medical Instrument Technology Co., Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
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Basic Information
- Brand Name
- Disposable Endoscope Injection Needle
- Primary DI
- 06936603226544
- Version / Model
- FTL-IN-24-230-19-5
- Catalog Number
- MMIN-19-5
- Company Name
- Yangzhou Fartley Medical Instrument Technology Co., Ltd
- Labeler DUNS
- 544375774
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2024-10-18
- Public Version
- 1
- Public Version Date
- 2024-10-28
- Public Version Status
- New
- Public Device Record Key
- d66747f5-7b33-4eda-b1f3-05d94e3fa255
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
- Labeling does not contain MRI Safety Information
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- No
- Has Lot/Batch Number
- Yes
- Has Manufacturing Date
- No
- 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 |
|---|---|---|---|---|
| FBK | Endoscopic Injection Needle, Gastroenterology-Urology | Gastroenterology, Urology | 876.1500 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 46678 | Flexible endoscopic biopsy handpiece/needle | A sterile flexible device intended to be used to obtain tissue specimens, for histopathological examination, during various endoscopic procedures (e.g., bronchoscopy, gastroscopy). It is typically constructed of a flexible metal coil or plastic tube whose distal end is equipped with a biopsy needle which is operated by a control handle attached at the proximal end of the instrument. It is introduced into the body cavity through an artificial orifice of the body or the working channel of the compatible endoscope. This is a single-use device. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 06936603226544 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| K220292 | 000 |