← Back to catalogue

Bl Offset Cup Impactor Universal

FDA UDI

Class II (US FDA UDI)

by Brainlab SE

Identity

Trade Name
Bl Offset Cup Impactor Universal FDA UDI
Generic Name
Robotic surgical navigation system FDA UDI
Model / Reference
52856B FDA UDI

Identifiers

Catalog Number
52856B FDA UDI
Primary DI / UDI-DI
04056481001940 FDA UDI
FDA Product Code
OLO FDA UDI
GMDN Term
Robotic surgical navigation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4560 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Bl Offset Cup Impactor Universal by Brainlab SE — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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
Brainlab SE

Sources (1)

  • FDA UDI 9faaea75-67d7-4dfd-a7e4-67e7b12ea813 35 fields · synced May 30, 2026