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Rusch

FDA UDI

Class I (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
RUSCH FDA UDI
Generic Name
Laryngoscope blade, single-use FDA UDI
Device Name
RUSCH GREENLITE SU MTL BLADE MAC 3 FDA UDI
Model / Reference
IPN915459 FDA UDI
Description
RUSCH GREENLITE SU MTL BLADE MAC 3 FDA UDI

Identifiers

Catalog Number
004551003 FDA UDI
Primary DI / UDI-DI
14026704711397 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Laryngoscope blade, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5540 FDA UDI
Commercial Distribution
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

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Laryngoscope blade, single-use

Rusch by Teleflex Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope blade, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Teleflex Incorporated

Sources (1)

  • FDA UDI 5795ccb2-1344-4af9-a122-7749341e92b1 36 fields · synced May 30, 2026