Identity
- Trade Name
- Sheathes FDA UDI
- Generic Name
- Body-orifice ultrasound imaging transducer cover, basic, non-sterile FDA UDI
- Device Name
- Latex, 0.5"D x 2.3"L, Non-Sterile, Ultrasound Probe Cover, Rectal, Seamless, Straight, Rolled FDA UDI
- Model / Reference
- 10090 FDA UDI
- Description
- Latex, 0.5"D x 2.3"L, Non-Sterile, Ultrasound Probe Cover, Rectal, Seamless, Straight, Rolled FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10842418100081 FDA UDI
- 510(k) Number
- K925869 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
Yes
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.
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- Non-Sterile Latex Endocavity Probe Cover — PROTEK MEDICAL PRODUCTS, INC. · Class II
- Rolled Probe Cover and Bands — PROTEK MEDICAL PRODUCTS, INC. · Class II
- MICROTEK — Microtek Medical LLC · Class II
- Non-Sterile Latex Endocavity Probe Cover — PROTEK MEDICAL PRODUCTS, INC. · Class II
Cleared under the same submission
K925869 also covers:
- Sheathes — Sheathing Technologies, Inc.
- Sheathes — Sheathing Technologies, Inc.
- Sheathes — Sheathing Technologies, Inc.
- Sheathes — Sheathing Technologies, Inc.
- Sheathes — Sheathing Technologies, Inc.
- Sheathes — Sheathing Technologies, Inc.
- Sheathes — Sheathing Technologies, Inc.
- Sheathes — Sheathing Technologies, Inc.
- Sheathes — Sheathing Technologies, Inc.
- Sheathes — Sheathing Technologies, Inc.
- Sheathes — Sheathing Technologies, Inc.
- Sheathes — Sheathing Technologies, Inc.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Sheathing Technologies, Inc.
Sources (1)
- FDA UDI cc3f3403-8aef-4363-97bc-3ab17c080dd4 34 fields · synced Jun 9, 2026