Identity
- Trade Name
- Polyp Collection Kit FDA UDI
- Generic Name
- Surgical suction system collection container, single-use FDA UDI
- Device Name
- The product is used to collect tissue samples of the diameter larger than 1mm and can be drawn through the endoscope through the suction device, which can be used for pathological analysis. FDA UDI
- Model / Reference
- BBP-50 FDA UDI
- Description
- The product is used to collect tissue samples of the diameter larger than 1mm and can be drawn through the endoscope through the suction device, which can be used for pathological analysis. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06932503554015 FDA UDI
- FDA Product Code
- KDQ FDA UDI
- GMDN Term
- Surgical suction system collection container, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.6740 FDA UDI
- Commercial Distribution
- 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
Category: Surgical suction system collection container, single-use
Polyp Collection Kit by Micro-Tech (Nanjing) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Micro-Tech (Nanjing) Co., Ltd.
Sources (1)
- FDA UDI e9e53608-15cc-41eb-84b1-21f15a92e5eb 34 fields · synced May 30, 2026