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Tyrx™

FDA UDI

Class II (US FDA UDI)

by Medtronic, Inc.

Identity

Trade Name
TYRX™ FDA UDI
Generic Name
Implantable pulse generator mesh bag, bioabsorbable FDA UDI
Device Name
ENVELOPE NMRM6122 ABSORB MED US MKT FDA UDI
Model / Reference
NMRM6122 FDA UDI
Description
ENVELOPE NMRM6122 ABSORB MED US MKT FDA UDI

Identifiers

Primary DI / UDI-DI
00643169983533 FDA UDI
510(k) Number
K150291 FDA UDI
FDA Product Code
FTL FDA UDI
GMDN Term
Implantable pulse generator mesh bag, bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3300 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

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Implantable pulse generator mesh bag, bioabsorbable

Tyrx™ by Medtronic, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Implantable pulse generator mesh bag, bioabsorbable.

Cleared under the same submission

K150291 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtronic, Inc.

Sources (1)

  • FDA UDI 77d3e695-423a-4c8e-a739-060ce1307819 37 fields · synced May 31, 2026