Identity
- Trade Name
- QUIKsheath Barriers T-Bar Light Handle FDA UDI
- Generic Name
- Medical equipment/instrument drape, single-use FDA UDI
- Device Name
- duce contamination and cleanup time between patients for only pennies per sheath. Unique design pulls over light handles more easily for an effective barrier. Provides visual assurance of aseptic procedures. Sheaths measure 6.25" x 3". FDA UDI
- Model / Reference
- 70-19724 FDA UDI
- Description
- duce contamination and cleanup time between patients for only pennies per sheath. Unique design pulls over light handles more easily for an effective barrier. Provides visual assurance of aseptic procedures. Sheaths measure 6.25" x 3". FDA UDI
Identifiers
- Catalog Number
- 70-19724 FDA UDI
- Primary DI / UDI-DI
- 00723896009741 FDA UDI
- FDA Product Code
- PEM FDA UDI
- GMDN Term
- Medical equipment/instrument drape, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4370 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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Medical equipment/instrument drape, single-use
QUIKsheath Barriers T-Bar Light Handle by Practicon, 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
- Practicon, Inc.
Sources (1)
- FDA UDI d6426a5e-aa3f-4f97-bd60-5120b1d1af61 34 fields · synced May 29, 2026