Identity
- Trade Name
- SheathesTEE FDA UDI
- Generic Name
- Topical coupling gel, sterile FDA UDI
- Device Name
- Polyurethane, 0.7" Tapered to 1.6"W Over 3.7”L x 48"L, Non-Sterile, Ultrasound Probe Cover Gathered on Applicator Tube with 3 Elastics, 20ml Sterile Gel, Bite Block, & 2 Tape Strips FDA UDI
- Model / Reference
- 5-T4000NS FDA UDI
- Description
- Polyurethane, 0.7" Tapered to 1.6"W Over 3.7”L x 48"L, Non-Sterile, Ultrasound Probe Cover Gathered on Applicator Tube with 3 Elastics, 20ml Sterile Gel, Bite Block, & 2 Tape Strips FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10842418103860 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: Topical coupling gel, sterileBody-orifice ultrasound imaging transducer cover, basic, non-sterile
SheathesTEE by Sheathing Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Sheathing Technologies, Inc.
Sources (1)
- FDA UDI 7e9c676a-b04a-4b1a-a993-670fba92dbde 33 fields · synced Jun 9, 2026