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MEDRAD® Avanta Single Patient Disposable Set - Transducer Compatable

FDA UDI

Class II (US FDA UDI)

by Bayer Medical Care Inc.

Identity

Trade Name
MEDRAD® Avanta Single Patient Disposable Set - Transducer Compatable FDA UDI
Generic Name
Radiographic procedure tubing FDA UDI
Device Name
Avanta Single-Patient Disposable Set (SET,PKG,SPDS,AVA500SPATL,US FBPIV,MC,JA2) (85239082) FDA UDI
Model / Reference
AVA 500 SPAT L FDA UDI
Description
Avanta Single-Patient Disposable Set (SET,PKG,SPDS,AVA500SPATL,US FBPIV,MC,JA2) (85239082) FDA UDI

Identifiers

Catalog Number
AVA 500 SPAT L FDA UDI
Primary DI / UDI-DI
00616258010199 FDA UDI
510(k) Number
K050456 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

MEDRAD® Avanta Single Patient Disposable Set - Transducer Compatable by Bayer Medical Care Inc. — Class II — FDA UDI — listed in FDA GUDID

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

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Manufacturer

Sources (1)

  • FDA UDI 6e87636b-34e6-4ac5-8562-9d7519120942 36 fields · synced Jun 9, 2026