Identity
- Trade Name
- MT FDA UDI
- Generic Name
- Flexible endoscopic biopsy forceps, single-use FDA UDI
- Device Name
- New handle,Oval, without spike, ,Single outer sheath, ,FEP coated, Four-bar linkage,1.8*1200 mm FDA UDI
- Model / Reference
- NBF02-11018120 FDA UDI
- Description
- New handle,Oval, without spike, ,Single outer sheath, ,FEP coated, Four-bar linkage,1.8*1200 mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06932503540018 FDA UDI
- FDA Product Code
- FCL FDA UDI
- GMDN Term
- Flexible endoscopic biopsy forceps, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.1075 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Lumen/Inner Diameter — 2.0 Millimeter FDA UDILength — 120 Centimeter FDA UDI
Mt by Micro-Tech (Nanjing) Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Micro-Tech (Nanjing) Co., Ltd.
Sources (1)
- FDA UDI 536c53e6-c5c1-486c-b323-98bbb5642834 36 fields · synced Jun 8, 2026