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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Instrument management bag, sterile FDA UDI
Device Name
POUCH, INSTRUMENT, 3POCKET, INVISISHIELD FDA UDI
Model / Reference
DYNJSD1018L FDA UDI
Description
POUCH, INSTRUMENT, 3POCKET, INVISISHIELD FDA UDI

Identifiers

Catalog Number
DYNJSD1018L FDA UDI
Primary DI / UDI-DI
10080196762491 FDA UDI
FDA Product Code
KKX FDA UDI
GMDN Term
Instrument management bag, sterile 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

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

Category: Instrument management bag, sterile

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

Similar devices

Also classified as Instrument management bag, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eafde7a5-9fb6-4e08-93bc-e01930860988 36 fields · synced May 30, 2026