← Back to catalogue

4WEB Medical

FDA UDI

Class I (US FDA UDI)

by 4Web Medical, Inc.

Identity

Trade Name
4WEB Medical FDA UDI
Generic Name
Bone awl, reusable FDA UDI
Model / Reference
CSTS-SA-000004 FDA UDI

Identifiers

Catalog Number
CSTS-SA-000004 FDA UDI
Primary DI / UDI-DI
00812998038534 FDA UDI
FDA Product Code
HWJ FDA UDI
GMDN Term
Bone awl, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Bone awl, reusable

4WEB Medical by 4Web Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone awl, reusable.

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
4Web Medical, Inc.

Sources (1)

  • FDA UDI 5bc77c8f-e31f-4cae-b5a5-09c2aeaf1e68 33 fields · synced May 31, 2026