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Peca® 4

FDA UDI

Class I (US FDA UDI)

by Novastep

Identity

Trade Name
PECA® 4 FDA UDI
Generic Name
Cannulated surgical drill bit, reusable FDA UDI
Device Name
Compressive Ø3,7 countersink FDA UDI
Model / Reference
XRE01023 FDA UDI
Description
Compressive Ø3,7 countersink FDA UDI

Identifiers

Catalog Number
XRE01023 FDA UDI
Primary DI / UDI-DI
03700879513300 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Cannulated surgical drill bit, reusable 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: Cannulated surgical drill bit, reusable

Peca® 4 by Novastep — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cannulated surgical drill bit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novastep

Sources (1)

  • FDA UDI 3c44257a-38ef-4b73-bdb4-a370ea03d407 35 fields · synced Jun 8, 2026