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Paul Banditt

FDA UDI

Class I (US FDA UDI)

by Terlain Enterprises, Inc.

Identity

Trade Name
Paul Banditt FDA UDI
Generic Name
Orthopaedic cement spatula FDA UDI
Device Name
Paul Banditt 22 Spatula, SE FDA UDI
Model / Reference
SPA22 FDA UDI
Description
Paul Banditt 22 Spatula, SE FDA UDI

Identifiers

Primary DI / UDI-DI
D955SPA221 FDA UDI
FDA Product Code
GAF FDA UDI
GMDN Term
Orthopaedic cement spatula FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

No

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

No

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: Orthopaedic cement spatula

Paul Banditt by Terlain Enterprises, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic cement spatula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 36bd73e0-364b-4180-80e8-4a472ff63082 33 fields · synced May 30, 2026