Identity
- Trade Name
- ACE FDA UDI
- Generic Name
- Instrument/equipment drape, single-use, non-sterile FDA UDI
- Device Name
- POWER UNIT DRAPE NON STERILE 24X24 L/F CASE ONLY 100/CA FDA UDI
- Model / Reference
- 0033138NS FDA UDI
- Description
- POWER UNIT DRAPE NON STERILE 24X24 L/F CASE ONLY 100/CA FDA UDI
Identifiers
- Catalog Number
- 0033138NS FDA UDI
- Primary DI / UDI-DI
- 00614950000036 FDA UDI
- FDA Product Code
- KKX FDA UDI
- GMDN Term
- Instrument/equipment drape, single-use, non-sterile 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
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Width — 24 Inch FDA UDILength — 24 Inch FDA UDI
Category: Instrument/equipment drape, single-use, non-sterile
Ace by Ace Surgical Supply Co., 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
- Ace Surgical Supply Co., Inc.
Sources (1)
- FDA UDI 707a9dc4-780e-44f9-a6b1-1c557089ae41 36 fields · synced May 30, 2026