← Back to catalogue

Surjex

FDA UDI

Class I (US FDA UDI)

by Surjex

Identity

Trade Name
Surjex FDA UDI
Generic Name
Bone holding forceps FDA UDI
Device Name
Pcs Bone Holding Clamp 5-1/2" Angled Serrected, FDA UDI
Model / Reference
WM3241113 FDA UDI
Description
Pcs Bone Holding Clamp 5-1/2" Angled Serrected, FDA UDI

Identifiers

Primary DI / UDI-DI
G383BONEHOLDINGCLAMPRQ5 FDA UDI
FDA Product Code
GEN FDA UDI
GMDN Term
Bone holding forceps 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Bone holding forceps

Surjex by Surjex — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone holding forceps.

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
Surjex

Sources (1)

  • FDA UDI 353aae5b-a02d-4787-985b-fcd1c4d42d6f 33 fields · synced May 31, 2026