← Back to catalogue

36M - Peco - Metal

FDA UDI

Class U (US FDA UDI)

by Certified Safety Manufacturing, Inc.

Identity

Trade Name
36M - Peco - Metal FDA UDI
Generic Name
Non-rebreathing valve, single-use FDA UDI
Device Name
36M - Peco - Metal FDA UDI
Model / Reference
K621-007 FDA UDI
Description
36M - Peco - Metal FDA UDI

Identifiers

Catalog Number
K621-007 FDA UDI
Primary DI / UDI-DI
00766588210070 FDA UDI
FDA Product Code
EFQ FDA UDI
CBP FDA UDI
HMP FDA UDI
LRR FDA UDI
KGX FDA UDI
GMDN Term
Non-rebreathing valve, single-use FDA UDI

Classification

Device Class
U FDA UDI
Regulation Number
868.5870 FDA UDI
878.4440 FDA UDI
880.5240 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

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: First aid kit, medicatedAdhesive bandageNon-woven gauze padDressing-fixation skin adhesive tape, non-silicone

36M - Peco - Metal by Certified Safety Manufacturing, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Eye pad.

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

Sources (1)

  • FDA UDI 6a3ca9d3-1507-4942-a083-730bcb498bf3 35 fields · synced May 30, 2026