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Jaeger

FDA UDI

Class I (US FDA UDI)

by Jaeger Medical GmbH

Identity

Trade Name
Jaeger FDA UDI
Generic Name
Nose clip, single-use FDA UDI
Device Name
Nose Clip Qty: 1 pack of 10 FDA UDI
Model / Reference
V-892900 FDA UDI
Description
Nose Clip Qty: 1 pack of 10 FDA UDI

Identifiers

Catalog Number
V-892900 FDA UDI
Primary DI / UDI-DI
14250892901135 FDA UDI
FDA Product Code
BXJ FDA UDI
GMDN Term
Nose clip, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6225 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Jaeger 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 03b084c0-5c65-4178-b06d-8730b410155c 37 fields · synced May 30, 2026