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Microtek

FDA UDI

Class II (US FDA UDI)

by Microtek Medical LLC

Identity

Trade Name
MICROTEK FDA UDI
Generic Name
Surgical tissue/fluid collection bag, non-sterile FDA UDI
Device Name
SUTURE BAG W/TAPE, 8" X 15" FDA UDI
Model / Reference
1 FDA UDI
Description
SUTURE BAG W/TAPE, 8" X 15" FDA UDI

Identifiers

Primary DI / UDI-DI
00748426001859 FDA UDI
FDA Product Code
PUI FDA UDI
GMDN Term
Surgical tissue/fluid collection bag, non-sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

No

FDA UDI

Category: Surgical tissue/fluid collection bag, non-sterile

Microtek by Microtek Medical LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical tissue/fluid collection bag, non-sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Microtek Medical LLC

Sources (1)

  • FDA UDI 2cc8c1ef-fe6f-426f-af91-7b1cb8f12e43 35 fields · synced Jun 8, 2026