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Sheathes

FDA UDI

Class II (US FDA UDI)

by Sheathing Technologies, Inc.

Identity

Trade Name
Sheathes FDA UDI
Generic Name
Topical coupling gel, sterile FDA UDI
Device Name
Polyurethane, 6"W x 48"L, Non-Sterile, Extended Field Ultrasound Probe & Cord Cover with 20ml Sterile Gel & 2 Elastics, Rolled FDA UDI
Model / Reference
5-486NS TVS FDA UDI
Description
Polyurethane, 6"W x 48"L, Non-Sterile, Extended Field Ultrasound Probe & Cord Cover with 20ml Sterile Gel & 2 Elastics, Rolled FDA UDI

Identifiers

Primary DI / UDI-DI
10842418103983 FDA UDI
FDA Product Code
OIP FDA UDI
GMDN Term
Topical coupling gel, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1680 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

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

No

FDA UDI

Category: Body-surface ultrasound imaging transducer coverTopical coupling gel, sterile

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

Similar devices

Also classified as Topical coupling gel, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 22b4be54-e1dc-49d3-a801-0216ed36e966 33 fields · synced Jun 9, 2026