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Mt

FDA UDI

Class II (US FDA UDI)

by Micro-Tech (Nanjing) Co., Ltd.

Identity

Trade Name
MT FDA UDI
Generic Name
Gastrointestinal endoscopic clip, long-term, non-bioabsorbable FDA UDI
Device Name
Open width11±1mm the max OD of insertion part 2.6mm working length 1950mm coated, single pickling wire, 10 pcs in the box FDA UDI
Model / Reference
LOCK-D-26-195-C-N FDA UDI
Description
Open width11±1mm the max OD of insertion part 2.6mm working length 1950mm coated, single pickling wire, 10 pcs in the box FDA UDI

Identifiers

Primary DI / UDI-DI
06932503530859 FDA UDI
510(k) Number
K202333 FDA UDI
FDA Product Code
PKL FDA UDI
GMDN Term
Gastrointestinal endoscopic clip, long-term, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4400 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

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
Length — 195 Centimeter FDA UDI
Outer Diameter — 2.6 Millimeter FDA UDI

Mt by Micro-Tech (Nanjing) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K202333 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Micro-Tech (Nanjing) Co., Ltd.

Sources (1)

  • FDA UDI 859e80df-dff8-448b-b919-be269d149d74 37 fields · synced May 31, 2026