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Zksk

FDA UDI

Class II (US FDA UDI)

by Beijing ZKSK Technology Co., Ltd

Identity

Trade Name
ZKSK FDA UDI
Generic Name
General-purpose endoscopic needle, single-use FDA UDI
Device Name
Endoscopic Injection Needle FDA UDI
Model / Reference
SN18-09/195-4 FDA UDI
Description
Endoscopic Injection Needle FDA UDI

Identifiers

Primary DI / UDI-DI
06934415067430 FDA UDI
510(k) Number
K213239 FDA UDI
FDA Product Code
FBK FDA UDI
GMDN Term
General-purpose endoscopic needle, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

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

Category: General-purpose endoscopic needle, single-use

Zksk by Beijing ZKSK Technology Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose endoscopic needle, single-use.

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 e0f9de2d-ba1b-4871-b525-2803e3f3a449 35 fields · synced May 30, 2026