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Zimmer® Trabecular Metaltm Reverse Shoulder System Instrumentation Tecomet Reame

FDA UDI

Class I (US FDA UDI)

by Symmetry Medical

Identity

Trade Name
ZIMMER® TRABECULAR METALTM REVERSE SHOULDER SYSTEM INSTRUMENTATION TECOMET REAME FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Model / Reference
00-4361-084-00 FDA UDI

Identifiers

Catalog Number
11-167-001 FDA UDI
Primary DI / UDI-DI
00847538004083 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting 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

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical instrument handle, non-torque-limiting

Zimmer® Trabecular Metaltm Reverse Shoulder System Instrumentation Tecomet Reame by Symmetry Medical — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Symmetry Medical

Sources (1)

  • FDA UDI 6337d925-6d40-42b8-8969-5583b0a64b5f 34 fields · synced Jun 8, 2026