MT
- Primary DI
- 16932503525111
- Brand
- MT
- Company
- Micro-Tech (Nanjing) Co., Ltd.
- Model
- DG-18-08-21
- Device description
- The diameter of the spring tip is 1.8mm, the diameter of the wire guide rod is 0.8mm, and the effective working length is 2100mm.
- Published
- 2021-12-31
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| OCY | Endoscopic Guidewire, Gastroenterology-Urology |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| OCY | Endoscopic Guidewire, Gastroenterology-Urology | Gastroenterology, Urology | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 16932503525111 | Package | GS1 | 10 | In Commercial Distribution |
| 26932503525118 | Package | GS1 | 25 | In Commercial Distribution |
| 06932503525114 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 16932503525111 | 16932503525111 | |
| 26932503525118 | 26932503525118 | |
| 06932503525114 | 06932503525114 | 6932503525114 |
GMDN Terms
| Term | Definition |
|---|---|
| Endoscopic-access dilator, single-use | A device intended to be used to dilate a body lumen or access channel to facilitate the introduction of endoscopic instruments percutaneously (through the skin) or through a natural orifice (e.g., urethra). It may be a flexible or rigid rod/tube with a tapered distal tip. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Guidewire Diameter | 0.8 | Millimeter |
| Guidewire Length | 2100 | Millimeter |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| 877-552-4027 | info@micro-tech-usa.com |
Regulatory Flags
- DUNS number
- 530269083
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
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|---|---|---|---|---|
| 16932503514658 | Biliary Plastic Stent Set | BPDS-41114-0712/17 | 2026-03-20 | |
| 16932503515617 | Biliary Plastic Stent Set | BPDS-41114-0715/17 | 2026-03-20 | |
| 16932503515624 | Biliary Plastic Stent Set | BPDS-41114-0718/17 | 2026-03-20 | |
| 16932503515631 | Biliary Plastic Stent Set | BPDS-41114-0805/22 | 2026-03-20 | |
| 16932503515648 | Biliary Plastic Stent Set | BPDS-41114-0807/22 | 2026-03-20 | |
| 16932503515655 | Biliary Plastic Stent Set | BPDS-41114-0809/22 | 2026-03-20 | |
| 16932503515662 | Biliary Plastic Stent Set | BPDS-41114-0812/22 | 2026-03-20 | |
| 16932503515679 | Biliary Plastic Stent Set | BPDS-41114-0815/22 | 2026-03-20 | |
| 16932503515686 | Biliary Plastic Stent Set | BPDS-41114-0818/22 | 2026-03-20 | |
| 16932503515693 | Biliary Plastic Stent Set | BPDS-41114-1005/22 | 2026-03-20 | |
| 16932503515709 | Biliary Plastic Stent Set | BPDS-41114-1007/22 | 2026-03-20 | |
| 16932503515716 | Biliary Plastic Stent Set | BPDS-41114-1009/22 | 2026-03-20 | |
| 16932503515723 | Biliary Plastic Stent Set | BPDS-41114-1012/22 | 2026-03-20 | |
| 16932503515730 | Biliary Plastic Stent Set | BPDS-41114-1015/22 | 2026-03-20 | |
| 16932503515747 | Biliary Plastic Stent Set | BPDS-41114-1018/22 | 2026-03-20 | |
| 16932503515754 | Biliary Plastic Stent Set | BPDS-41114-1105/22 | 2026-03-20 | |
| 16932503515761 | Biliary Plastic Stent Set | BPDS-41114-1107/22 | 2026-03-20 | |
| 16932503515778 | Biliary Plastic Stent Set | BPDS-41114-1109/22 | 2026-03-20 | |
| 16932503515785 | Biliary Plastic Stent Set | BPDS-41114-1112/22 | 2026-03-20 | |
| 16932503515792 | Biliary Plastic Stent Set | BPDS-41114-1115/22 | 2026-03-20 |
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