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Litetouch Medium Mask
EUDAMEDFDA UDIClass I (EU MDR)
Ref 1082715Model LiteTouch Medium Mask/Masque Moyen
Identity
- Trade Name
- LITETOUCH MEDIUM MASK EUDAMEDLiteTouch Medium Mask/Masque Moyen EUDAMEDLiteTouch FDA UDI
- Generic Name
- Medicine chamber spacer, reusable FDA UDI
- Device Name
- LiteTouch Face Mask EUDAMEDLiteTouch Medium Mask, 10-pack. FDA UDI
- Model / Reference
- 1082715 EUDAMEDLiteTouch Medium Mask/Masque Moyen EUDAMED00 FDA UDI
- Description
- LiteTouch Medium Mask, 10-pack. FDA UDI
Identifiers
- Catalog Number
- 1082715 FDA UDI
- Primary DI / UDI-DI
- 00383730000770 EUDAMEDFDA UDI
- Basic UDI-DI
- 038373BM262XD EUDAMEDB-00383730000770 EUDAMED
- FDA Product Code
- CAF FDA UDI
- EMDN Code
- R030199 RESPIRATORY MASKS - OTHER EUDAMED
- GMDN Term
- Medicine chamber spacer, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 868.5630 FDA UDI
- Market of Registration
- Belgium EUDAMEDAustria EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Anaesthesia face mask, single-use
Litetouch Medium Mask by Respironics, Inc. — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Also classified as Anaesthesia face mask, single-use.
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- Ventlab — Ventlab Corp. · Class I
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- King Mask — Ambu A/S · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | 038373BM262XD | Class I | Active |
| EUDAMED | European Union | CE/MDR | 038373BM262XD | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Respironics Inc.
- EUDAMED SRN
- US-MF-000002301
- Authorised Representative
- Philips Medical Systems Nederland B.V. NL-AR-000001422
Sources (3)
- EUDAMED 64e7ead8-9299-4aa2-8675-bfb105dd38af 61 fields · synced Jun 20, 2026
- FDA UDI 503a4633-ca25-43a5-8926-69b9f43c0cfc 35 fields · synced May 30, 2026
- EUDAMED fd00eebe-c142-4e5b-9289-941a36059771 61 fields · synced Jun 20, 2026