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Antmed

FDA UDI

Class II (US FDA UDI)

by ShenZhen Antmed Co., Ltd

Identity

Trade Name
Antmed FDA UDI
Generic Name
Radiographic procedure tubing FDA UDI
Device Name
Connecting Tubes FDA UDI
Model / Reference
630250 FDA UDI
Description
Connecting Tubes FDA UDI

Identifiers

Primary DI / UDI-DI
06945764412208 FDA UDI
FDA Product Code
DQO FDA UDI
GMDN Term
Radiographic procedure tubing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 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

Category: Radiographic procedure tubing

Antmed by ShenZhen Antmed Co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiographic procedure tubing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0e8d58a8-4bc4-4043-8153-cfc363babea6 34 fields · synced Jun 8, 2026