← Back to catalogue

Sinton Medical Products

FDA UDI

Class II (US FDA UDI)

by Shenzhen Boon Medical Supply Co., Ltd.

Identity

Trade Name
Sinton Medical Products FDA UDI
Generic Name
Radiographic procedure tubing FDA UDI
Device Name
1-60"(1500mm) Straight Tubing with Check Valve FDA UDI
Model / Reference
400101-20 FDA UDI
Description
1-60"(1500mm) Straight Tubing with Check Valve FDA UDI

Identifiers

Catalog Number
HT-L1501 FDA UDI
Primary DI / UDI-DI
06938327902988 FDA UDI
510(k) Number
K241109 FDA UDI
FDA Product Code
DXT FDA UDI
GMDN Term
Radiographic procedure tubing FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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

Sinton Medical Products by Shenzhen Boon Medical Supply Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiographic procedure tubing.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 5706d9db-2f0e-4997-a0f7-54501d845116 37 fields · synced Jun 1, 2026