← Back to catalogue

Maxbraid

FDA UDI

Class II (US FDA UDI)

by Biomet Sports Medicine

Identity

Trade Name
MAXBRAID FDA UDI
Generic Name
Polyolefin/fluoropolymer suture, multifilament FDA UDI
Model / Reference
900337 FDA UDI

Identifiers

Catalog Number
900337 FDA UDI
Primary DI / UDI-DI
00880304464940 FDA UDI
510(k) Number
K040472 FDA UDI
FDA Product Code
GAT FDA UDI
GMDN Term
Polyolefin/fluoropolymer suture, multifilament FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5000 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Polyolefin/fluoropolymer suture, multifilament

Maxbraid by Biomet Sports Medicine — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polyolefin/fluoropolymer suture, multifilament.

Cleared under the same submission

K040472 also covers:

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
Biomet Sports Medicine

Sources (1)

  • FDA UDI 6ab3f5f7-c332-4a3a-a08a-7a02a2d80579 35 fields · synced May 30, 2026