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Intuit SnapFIT Transducer Cover

FDA UDIEUDAMED

Class II (US FDA UDI)

by Civco Medical Instruments Co., Inc.

Identity

Trade Name
Intuit SnapFIT Transducer Cover FDA UDI
Generic Name
Body-surface ultrasound imaging transducer cover FDA UDI
Device Name
Sterile (14x30cm) CIV-Flex cover with applicator with PEELSafe Advantage FDA UDI
Model / Reference
610-2290, 610-2290-5 FDA UDI
Description
Sterile (14x30cm) CIV-Flex cover with applicator with PEELSafe Advantage FDA UDI

Identifiers

Catalog Number
610-2290, 610-2290-5 FDA UDI
Primary DI / UDI-DI
10841436111833 FDA UDI
510(k) Number
K970513 FDA UDI
FDA Product Code
ITX FDA UDI
GMDN Term
Body-surface ultrasound imaging transducer cover FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 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

Yes

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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Body-surface ultrasound imaging transducer cover

Intuit SnapFIT Transducer Cover by Civco Medical Instruments Co., Inc. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Body-surface ultrasound imaging transducer cover.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI aae22123-f41b-4254-8c01-0e9690bd878b 37 fields · synced Oct 7, 2026
  • EUDAMED 1 fields · synced Jun 19, 2026