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Dukal

FDA UDI

Class I (US FDA UDI)

by Dukal LLC

Identity

Trade Name
Dukal FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Air Water Syringe Sleeve, 2-1/2" X 10" FDA UDI
Model / Reference
27608 FDA UDI
Description
Air Water Syringe Sleeve, 2-1/2" X 10" FDA UDI

Identifiers

Catalog Number
27608 FDA UDI
Primary DI / UDI-DI
10665973027255 FDA UDI
FDA Product Code
NRD FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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

Yes

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

Category: Medical equipment/instrument drape, single-use

Dukal by Dukal LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dukal LLC

Sources (1)

  • FDA UDI 7fd4a487-0d11-4d38-8a42-fecbe32269b6 35 fields · synced Jun 8, 2026