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Lf

FDA UDI

Class II (US FDA UDI)

by Shenzhen Boon Medical Supply Co., Ltd.

Identity

Trade Name
LF FDA UDI
Generic Name
Angiographic syringe FDA UDI
Device Name
150mL Angiographic Syringe with Large Spike; fits injector: Angiomat Illumena FDA UDI
Model / Reference
300103-A FDA UDI
Description
150mL Angiographic Syringe with Large Spike; fits injector: Angiomat Illumena FDA UDI

Identifiers

Catalog Number
900103S FDA UDI
Primary DI / UDI-DI
06938327903237 FDA UDI
510(k) Number
K151960 FDA UDI
FDA Product Code
DXT FDA UDI
GMDN Term
Angiographic syringe 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: Angiographic syringe

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

Similar devices

Also classified as Angiographic syringe.

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 4075d0cb-dfa5-49e0-bbb8-8e5894110d39 37 fields · synced Jun 8, 2026