← Back to catalogue

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
SANI SLEEVE 2X60" STER 10/PKG L/F FDA UDI
Model / Reference
6411000 FDA UDI
Description
SANI SLEEVE 2X60" STER 10/PKG L/F FDA UDI

Identifiers

Catalog Number
6411000 FDA UDI
Primary DI / UDI-DI
00614950007059 FDA UDI
FDA Product Code
MMP 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 — 60 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Ace Surgical Supply Co., Inc.

Sources (1)

  • FDA UDI a4477cb2-0066-4f53-9744-8a42014155a6 36 fields · synced Jun 1, 2026