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Unbranded

FDA UDI

Class II (US FDA UDI)

by Advance Medical Designs, Inc.

Identity

Trade Name
UNBRANDED FDA UDI
Generic Name
Instrument/equipment drape, single-use, sterile FDA UDI
Device Name
Snap Kover FDA UDI
Model / Reference
01-1010 FDA UDI
Description
Snap Kover FDA UDI

Identifiers

Primary DI / UDI-DI
00848340000072 FDA UDI
FDA Product Code
JAA FDA UDI
GMDN Term
Instrument/equipment drape, single-use, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1650 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Instrument/equipment drape, single-use, sterile

Unbranded by Advance Medical Designs, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument/equipment drape, single-use, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Advance Medical Designs, Inc.

Sources (1)

  • FDA UDI 7a3b18a5-285a-4bea-ab40-58f6e15e35b7 33 fields · synced Jun 8, 2026