← Back to catalogue

Sonic Window Sterile Transducer Cover

FDA UDI

Class II (US FDA UDI)

by Analogic Corporation

Identity

Trade Name
Sonic Window Sterile Transducer Cover FDA UDI
Generic Name
Hand-held ultrasound imaging system, body-surface FDA UDI
Device Name
Sterile Transducer Cover - individual cover in envelope FDA UDI
Model / Reference
21-05012-01 FDA UDI
Description
Sterile Transducer Cover - individual cover in envelope FDA UDI

Identifiers

Primary DI / UDI-DI
90814277020127 FDA UDI
510(k) Number
K140126 FDA UDI
FDA Product Code
ITX FDA UDI
IYN FDA UDI
IYO FDA UDI
GMDN Term
Hand-held ultrasound imaging system, body-surface FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
892.1550 FDA UDI
892.1560 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Hand-held ultrasound imaging system, body-surface

Sonic Window Sterile Transducer Cover by Analogic Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held ultrasound imaging system, body-surface.

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 e42cf25f-ff6c-4715-89fa-feed633e5c64 35 fields · synced May 30, 2026