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SureClip

FDA UDI

Class II (US FDA UDI)

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

Identity

Trade Name
SureClip FDA UDI
Generic Name
Gastrointestinal endoscopic clip, short-term FDA UDI
Device Name
Open width16±2mm the max OD of insertion part 2.6mm working length 2700mm coated FDA UDI
Model / Reference
ROCC-F-26-270-C FDA UDI
Description
Open width16±2mm the max OD of insertion part 2.6mm working length 2700mm coated FDA UDI

Identifiers

Catalog Number
ROCC-F-26-270-C FDA UDI
Primary DI / UDI-DI
06932503530323 FDA UDI
FDA Product Code
PKL FDA UDI
GMDN Term
Gastrointestinal endoscopic clip, short-term 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d3e1453a-b0b9-4ced-b22d-c36f4eab981d 35 fields · synced Jun 1, 2026