← Back to catalogue

V. Mueller

FDA UDI

Class I (US FDA UDI)

by Steris Corporation

Identity

Trade Name
V. Mueller FDA UDI
Generic Name
Nasal scissors FDA UDI
Device Name
V. Mueller Pediatric Nasal Scissors Right Blade Length 5.5 MM OL 5 7/8-inch (150MM) SL 4 3/8-inch (l00 MM) FDA UDI
Model / Reference
RH551-152 FDA UDI
Description
V. Mueller Pediatric Nasal Scissors Right Blade Length 5.5 MM OL 5 7/8-inch (150MM) SL 4 3/8-inch (l00 MM) FDA UDI

Identifiers

Catalog Number
RH551152 FDA UDI
Primary DI / UDI-DI
10885403110252 FDA UDI
FDA Product Code
KBD FDA UDI
GMDN Term
Nasal scissors FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Nasal scissors

V. Mueller by Steris Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasal scissors.

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

Manufacturer
Steris Corporation

Sources (1)

  • FDA UDI 22a071d0-79e7-464a-946c-cfa217e98d15 35 fields · synced Jun 8, 2026