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Micro Medical

FDA UDI

Class I (US FDA UDI)

by Jaeger Medical GmbH

Identity

Trade Name
Micro Medical FDA UDI
Generic Name
Breathing mouthpiece, reusable FDA UDI
Device Name
ACC NASAL PROBE SET, Consits of 1 EA 36-NPROBE01 Extra Small Nasal Probes 1 EA 36-NPROBE02 Small Nasal Probes 1 EA 36-NPROBE03 Medium Nasal Probes 1 EA 36-NPROBE04 Large Nasal Probes FDA UDI
Model / Reference
36-NPROBE00 FDA UDI
Description
ACC NASAL PROBE SET, Consits of 1 EA 36-NPROBE01 Extra Small Nasal Probes 1 EA 36-NPROBE02 Small Nasal Probes 1 EA 36-NPROBE03 Medium Nasal Probes 1 EA 36-NPROBE04 Large Nasal Probes FDA UDI

Identifiers

Catalog Number
36-NPROBE00 FDA UDI
Primary DI / UDI-DI
14250892901708 FDA UDI
FDA Product Code
BYP FDA UDI
GMDN Term
Breathing mouthpiece, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5620 FDA UDI
Commercial Distribution
Not 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Micro Medical by Jaeger Medical GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Jaeger Medical GmbH

Sources (1)

  • FDA UDI e67de3e4-a0c1-4bb5-8f51-c958f35e6ebe 37 fields · synced May 30, 2026