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MicroSurge

FDA UDI

Class II (US FDA UDI)

by Med Michigan Holdings Llc

Identity

Trade Name
MicroSurge FDA UDI
Generic Name
Surgical irrigation tubing set, single-use FDA UDI
Device Name
BlowMister FDA UDI
Model / Reference
BLM-22150 FDA UDI
Description
BlowMister FDA UDI

Identifiers

Catalog Number
BLM-22150 FDA UDI
Primary DI / UDI-DI
00817278011993 FDA UDI
FDA Product Code
FQH FDA UDI
GMDN Term
Surgical irrigation tubing set, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5475 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

Yes

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Surgical irrigation tubing set, single-use

MicroSurge by Med Michigan Holdings Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation tubing set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 163f22ff-62f1-413a-b0cf-10402d2f1f83 34 fields · synced May 30, 2026