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Sheathes

FDA UDI

Class II (US FDA UDI)

by Sheathing Technologies, Inc.

Identity

Trade Name
Sheathes FDA UDI
Generic Name
Body-orifice ultrasound imaging transducer cover, basic, non-sterile FDA UDI
Device Name
Polyurethane, 7/8"D Tapered to 2.9"W x 11.8"L, Non-Sterile, Ultrasound Probe Cover, Vaginal/Rectal, Tapered, Rolled with Pull Tab, Extra-Long, Vital Care Industries Custom Label FDA UDI
Model / Reference
26339VCI FDA UDI
Description
Polyurethane, 7/8"D Tapered to 2.9"W x 11.8"L, Non-Sterile, Ultrasound Probe Cover, Vaginal/Rectal, Tapered, Rolled with Pull Tab, Extra-Long, Vital Care Industries Custom Label FDA UDI

Identifiers

Primary DI / UDI-DI
10842418102467 FDA UDI
FDA Product Code
ITX FDA UDI
GMDN Term
Body-orifice ultrasound imaging transducer cover, basic, non-sterile 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

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Body-orifice ultrasound imaging transducer cover, basic, non-sterile

Sheathes by Sheathing Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Body-orifice ultrasound imaging transducer cover, basic, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 671215d7-1f62-4c93-9936-216f081eee52 33 fields · synced Jun 9, 2026