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AD Surgical

FDA UDI

Class II (US FDA UDI)

by Applied Dental, Inc.

Identity

Trade Name
AD Surgical FDA UDI
Generic Name
Surgical dressing/drape kit, single-use FDA UDI
Device Name
Utility Drape Sterile, 22"x25". Absorbent, Impervious PE/PP. FDA UDI
Model / Reference
A400-UTD FDA UDI
Description
Utility Drape Sterile, 22"x25". Absorbent, Impervious PE/PP. FDA UDI

Identifiers

Primary DI / UDI-DI
00814639022087 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Surgical dressing/drape kit, 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical dressing/drape kit, single-use

AD Surgical by Applied Dental, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical dressing/drape kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2d2026da-7e7d-4f11-a8a0-da1eec5f0df4 34 fields · synced May 31, 2026