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Cannula

FDA UDI

Class II (US FDA UDI)

by Shanghai Kinetic Medical Co., Ltd.

Identity

Trade Name
Cannula FDA UDI
Generic Name
Bone access channel kit FDA UDI
Device Name
Dilator, 8G (4.2mm) FDA UDI
Model / Reference
FG2210 FDA UDI
Description
Dilator, 8G (4.2mm) FDA UDI

Identifiers

Catalog Number
FG2210 FDA UDI
Primary DI / UDI-DI
06938695537669 FDA UDI
510(k) Number
K113742 FDA UDI
FDA Product Code
HRX FDA UDI
NDN FDA UDI
GMDN Term
Bone access channel kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 FDA UDI
888.3027 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 4.2 Millimeter FDA UDI

Category: Bone access channel kit

Cannula by Shanghai Kinetic Medical Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone access channel kit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7fc834e1-45a3-481e-8b7c-af4828ee01f2 38 fields · synced May 30, 2026