TMM - SL-S (Tactical Medical Module - Saline Lock - Standard)

FDA UDI

Class II (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name: TMM - SL-S (Tactical Medical Module - Saline Lock - Standard) FDA UDI
Generic Name: Peripheral vascular catheter FDA UDI
Model / Reference: 3962 FDA UDI

Identifiers

Primary DI / UDI-DI: 00856767008113 FDA UDI
FDA Product Code: FOZ FDA UDI
GMDN Term: Peripheral vascular catheter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Peripheral vascular catheter

TMM - SL-S (Tactical Medical Module - Saline Lock - Standard) by Altitude Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Peripheral vascular catheter.

Arterial Line Kit — Argon Medical Devices, Inc. · Class I
DELTAVEN — DELTA MED SPA · Class II
EXEL Safelet Catheter — Exel International · Class II
Jelco — ICU MEDICAL, INC. · Class II
DELTAVEN — DELTA MED SPA · Class II
EXEL Safelet Catheter — Exel International · Class II
POWERWAND — ICU MEDICAL, INC. · Class II
POWERWAND — Access Scientific, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Altitude Technologies Inc.

Sources (1)

FDA UDI bd7f41e6-0015-4c00-b5ec-0577ecdc6097 32 fields · synced May 30, 2026