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Ace

FDA UDI

Class II (US FDA UDI)

by Ace Surgical Supply Co., Inc.

Identity

Trade Name
ACE FDA UDI
Generic Name
Instrument/equipment drape, reusable, sterile FDA UDI
Device Name
DRAPE ACE POWER CORD 3X96" STER L/F 5/PKG FDA UDI
Model / Reference
0033139 FDA UDI
Description
DRAPE ACE POWER CORD 3X96" STER L/F 5/PKG FDA UDI

Identifiers

Catalog Number
0033139 FDA UDI
Primary DI / UDI-DI
00614950000043 FDA UDI
FDA Product Code
KKX FDA UDI
GMDN Term
Instrument/equipment drape, reusable, 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 99 Inch FDA UDI

Category: Instrument/equipment drape, reusable, sterile

Ace by Ace Surgical Supply Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument/equipment drape, reusable, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ace Surgical Supply Co., Inc.

Sources (1)

  • FDA UDI 6614ad9f-c90d-4a52-864e-065f81c284dc 36 fields · synced Jun 8, 2026