← Back to catalogue

Tricera™ Handpiece

FDA UDI

Class II (US FDA UDI)

by RELIGN Corporation

Identity

Trade Name
Tricera™ Handpiece FDA UDI
Generic Name
Arthroscopic shaver system handpiece, electrically-powered FDA UDI
Device Name
Shaver Handpiece FDA UDI
Model / Reference
R-10002 FDA UDI
Description
Shaver Handpiece FDA UDI

Identifiers

Catalog Number
R-10002 FDA UDI
Primary DI / UDI-DI
00859273007021 FDA UDI
510(k) Number
K162770 FDA UDI
FDA Product Code
HRX FDA UDI
GEI FDA UDI
GMDN Term
Arthroscopic shaver system handpiece, electrically-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1100 FDA UDI
878.4400 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Hydrogen Peroxide FDA UDI
MRI Safety
MR Unsafe FDA UDI

Tricera™ Handpiece by RELIGN Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K162770 also covers:

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
RELIGN Corporation

Sources (1)

  • FDA UDI 910e9e20-45d4-4487-9dfc-f7638275a2b9 37 fields · synced Jun 9, 2026