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Puncture Aimer

FDA UDI

Class I (US FDA UDI)

by Well Lead Medical Co., Ltd

Identity

Trade Name
Puncture Aimer FDA UDI
Generic Name
Stationary x-ray grid FDA UDI
Device Name
Puncture Aimer FDA UDI
Model / Reference
U01C060110 FDA UDI
Description
Puncture Aimer FDA UDI

Identifiers

Primary DI / UDI-DI
06936881156632 FDA UDI
FDA Product Code
IXJ FDA UDI
GMDN Term
Stationary x-ray grid FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1910 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

Yes

FDA UDI

Category: Stationary x-ray grid

Puncture Aimer by Well Lead Medical Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Stationary x-ray grid.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI adf929b9-a9b2-4926-bc32-ef8c515dbbd0 33 fields · synced May 30, 2026