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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Surgical soft-tissue manipulation forceps, scissors-like, single-use FDA UDI
Device Name
5IN STRAIGHT MOSQUITO FORCEPS FDA UDI
Model / Reference
DYND04033 FDA UDI
Description
5IN STRAIGHT MOSQUITO FORCEPS FDA UDI

Identifiers

Catalog Number
DYND04033 FDA UDI
Primary DI / UDI-DI
40884389539454 FDA UDI
FDA Product Code
HTD FDA UDI
GMDN Term
Surgical soft-tissue manipulation forceps, scissors-like, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

FDA UDI

Category: Surgical soft-tissue manipulation forceps, scissors-like, single-use

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

Similar devices

Also classified as Surgical soft-tissue manipulation forceps, scissors-like, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e888399a-502f-4e18-b092-663af59d5d6b 35 fields · synced May 30, 2026