← Back to catalogue

Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Non-fixed blood collection needle FDA UDI
Device Name
STRIP,TEST,GLUCOSE,HARMONY FDA UDI
Model / Reference
MPH6550 FDA UDI
Description
STRIP,TEST,GLUCOSE,HARMONY FDA UDI

Identifiers

Catalog Number
MPH6550 FDA UDI
Primary DI / UDI-DI
10888277675681 FDA UDI
510(k) Number
K161299 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Non-fixed blood collection needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-fixed blood collection needle

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

Similar devices

Also classified as Non-fixed blood collection needle.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI bb72a1ba-3ef9-47b4-b3f0-0e289a566194 37 fields · synced May 30, 2026