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Halyard Scatter Radiation Shields

FDA UDI

Class I (US FDA UDI)

by Angiosystems, Incorporated

Identity

Trade Name
Halyard Scatter Radiation Shields FDA UDI
Generic Name
Patient radiation shielding pad/drape, single-use FDA UDI
Model / Reference
49020 Biliary Shield Drape L1 FDA UDI

Identifiers

Primary DI / UDI-DI
00816611026090 FDA UDI
FDA Product Code
KPY FDA UDI
GMDN Term
Patient radiation shielding pad/drape, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.6500 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient radiation shielding pad/drape, single-use

Halyard Scatter Radiation Shields by Angiosystems, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient radiation shielding pad/drape, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Angiosystems, Incorporated

Sources (1)

  • FDA UDI 9a339207-44cc-4675-893c-181048527f0c 32 fields · synced Jun 8, 2026