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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Ear canal irrigation kit, single-use FDA UDI
Device Name
SYRINGE,EAR/ULCER, 3 OZ, STERILE FDA UDI
Model / Reference
DYND70277 FDA UDI
Description
SYRINGE,EAR/ULCER, 3 OZ, STERILE FDA UDI

Identifiers

Catalog Number
DYND70277 FDA UDI
Primary DI / UDI-DI
10080196862542 FDA UDI
FDA Product Code
KYZ FDA UDI
GMDN Term
Ear canal irrigation kit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6960 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 90 Milliliter FDA UDI
Total Volume — 3 Fluid Ounce FDA UDI

Category: Ear canal irrigation kit, single-use

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ear canal irrigation kit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5fcb9840-d906-40b7-8ee4-509c8c96b6b1 36 fields · synced May 31, 2026