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Merlin

FDA UDIEUDAMED

Class I (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
MERLIN FDA UDI
Generic Name
Arthroscopic shaver system blade, single-use FDA UDI
Device Name
MERLIN FULL RADIUS, BENDABLE TO 30°, SHAVER BLADE, 3.7 MM FDA UDI
Model / Reference
P9375 FDA UDI
Description
MERLIN FULL RADIUS, BENDABLE TO 30°, SHAVER BLADE, 3.7 MM FDA UDI

Identifiers

Catalog Number
P9375 FDA UDI
Primary DI / UDI-DI
10845854036709 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Arthroscopic shaver system blade, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 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

No

FDA UDI

Category: Arthroscopic shaver system blade, single-use

Merlin by Conmed Corporation — Class I — MDD, MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic shaver system blade, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (2)

  • FDA UDI beec5407-af09-48a6-87f6-955b86670833 36 fields · synced Jun 18, 2026
  • EUDAMED 1 fields · synced Jun 4, 2026