AESCULAP
- Primary DI
- 04038653345038
- Brand
- AESCULAP
- Company
- Aesculap AG
- Model
- JG910
- Catalog number
- JG910
- Device description
- ANTIFOGGING SOLN.STERILE F.ENDOSCOPES
- Published
- 2020-05-20
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| KQM | CAMERA, SURGICAL AND ACCESSORIES |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| KQM | Camera, Surgical And Accessories | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 04046955606337 | Primary | GS1 | 0 | |
| 04038653345038 | Unit of Use | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 04046955606337 | 04046955606337 | 4046955606337 |
| 04038653345038 | 04038653345038 | 4038653345038 |
GMDN Terms#
| Term | Definition |
|---|---|
| Endoscope antifog solution | A liquid substance intended to be used to prevent the occurrence of condensed vapour (fog) on the lens of an endoscopic instrument during treatment. It will typically be used on the lens of an endoscopic camera where the warmth from an enclosed body cavity creates the conditions to produce fog on the lens. This device will typically be contained in a spray can, bottle, or squeeze bottle. After application, this device cannot be reused. |
Sterilization Methods#
| Method |
|---|
Contacts#
| Phone | |
|---|---|
| +1(800)282-9000 | GUDID.BBMUS_Service@bbraun.com |
Regulatory Flags#
- DUNS number
- 315018218
- Device count
- 20
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 04038653033997 | AESCULAP | DC230R | DC230R | 2020-06-17 |
| 04038653034321 | AESCULAP | DE112R | DE112R | 2020-06-17 |
| 04038653034369 | AESCULAP | DE116R | DE116R | 2020-06-17 |
| 04038653034376 | AESCULAP | DE117R | DE117R | 2020-06-17 |
| 04038653034406 | AESCULAP | DE120R | DE120R | 2020-06-17 |
| 04038653034901 | AESCULAP | DE676R | DE676R | 2020-06-17 |
| 04046963116194 | S4 CERVICAL | FW028U | FW028U | 2020-08-24 |
| 04046963794248 | ELAN 4 | GA768 | GA768 | 2020-04-24 |
| 04046963935184 | HI-LINE XXS | GE813SU | GE813SU | 2020-04-24 |
| 04046963935191 | HI-LINE XXS | GE814SU | GE814SU | 2020-04-24 |
| 04046963966362 | ELAN 4 | GA767 | GA767 | 2020-04-24 |
| 04046964054907 | ELAN 4 | GA715R | GA715R | 2020-04-24 |
| 04046964076664 | AESCULAP | GE812SU | GE812SU | 2020-04-24 |
| 04046964526213 | ECCOS | GB068R | GB068R | 2020-04-24 |
| 04038653013845 | AESCULAP | OP297R | OP297R | 2017-07-31 |
| 04038653081141 | AESCULAP | OP913 | OP913 | 2016-09-23 |
| 04038653081158 | AESCULAP | OP914 | OP914 | 2020-08-10 |
| 04038653013852 | AESCULAP | OP298R | OP298R | 2020-04-17 |
| 04046963730109 | AESCULAP | OP923 | OP923 | 2019-04-30 |
| 04046955273508 | AICON | JJ612 | JJ612 | 2022-02-25 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 00819761023063 | Optik View | LINDEN GROUP CORPORATION, THE | KQM | 2026-06-05 |
| 00819761023087 | Optik View | LINDEN GROUP CORPORATION, THE | KQM | 2026-06-05 |
| 00819761023094 | Optik View | LINDEN GROUP CORPORATION, THE | KQM | 2026-06-04 |
| 05415334053168 | Barco | Barco NV | KQM | 2026-06-02 |
| 05415334053335 | Barco | Barco NV | KQM | 2026-06-02 |
| 05415334056411 | Barco | Barco NV | KQM | 2026-06-02 |
| 05415334056428 | Barco | Barco NV | KQM | 2026-06-02 |
| 05415334056435 | Barco | Barco NV | KQM | 2026-06-02 |
| 05415334056442 | Barco | Barco NV | KQM | 2026-06-02 |
| 04995047074946 | CuratOR | EIZO CORPORATION | KQM | 2026-05-29 |
| 03700712438524 | Maquet Orchide | MAQUET SAS | KQM | 2026-05-11 |
| 00810000890675 | Arthrex | FORESEESON CUSTOM DISPLAYS, INC. | KQM | 2026-05-08 |
| 03700712434472 | Maquet Orchide | MAQUET SAS | KQM | 2026-05-06 |
| 03700712434489 | Maquet Orchide | MAQUET SAS | KQM | 2026-05-06 |
| 04548736183407 | SONY | SONY CORPORATION | KQM | 2026-04-30 |
| 04548736183414 | SONY | SONY CORPORATION | KQM | 2026-04-30 |
| 00860014850509 | HMDmd Wearable Surgical Monitor | HMDMD INC. | KQM | 2025-11-22 |
| 04548736155978 | SONY | SONY CORPORATION | KQM | 2025-11-04 |
| 04548736155985 | SONY | SONY CORPORATION | KQM | 2025-11-04 |
| 04548736169968 | SONY | SONY CORPORATION | KQM | 2025-11-04 |
| 04548736169951 | SONY | SONY CORPORATION | KQM | 2025-10-06 |
| 04548736155091 | SONY | SONY CORPORATION | KQM | 2025-09-30 |
| 04548736155107 | SONY | SONY CORPORATION | KQM | 2025-09-30 |
| 04548736170735 | SONY | SONY CORPORATION | KQM | 2025-09-30 |
| 04548736170759 | SONY | SONY CORPORATION | KQM | 2025-09-30 |
| 00848657077729 | AED ENDOPRO® PRIMO SERIES CAMERA | NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. | KQM | 2025-09-25 |
| 10618125114662 | Sirona | TIDI PRODUCTS, LLC | KQM | 2025-07-10 |
| 04548736170681 | SONY | SONY CORPORATION | KQM | 2025-06-24 |
| 04548736170704 | SONY | SONY CORPORATION | KQM | 2025-06-24 |
| 00848657077088 | AED ENDOPRO® PRIMO SERIES CAMERA | NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. | KQM | 2025-01-09 |